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nsv482886

  • Variant Calls:20
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:178,824

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 990 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):392,250-571,073Question Mark
Overlapping variant regions from other studies: 990 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):342,250-521,073Question Mark
Submitted genomic332,250-511,073Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv482886RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8392,250571,073
nsv482886RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8342,250521,073
nsv482886Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000008.8Chr8332,250511,073

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv3006781sequence alterationBAC aCGHProbe signal intensity
nssv3006886sequence alterationBAC aCGHProbe signal intensity
nssv3006916sequence alterationBAC aCGHProbe signal intensity
nssv3007700sequence alterationBAC aCGHProbe signal intensity
nssv3007790sequence alterationBAC aCGHProbe signal intensity
nssv3007856sequence alterationBAC aCGHProbe signal intensity
nssv3007911sequence alterationBAC aCGHProbe signal intensity
nssv3008198sequence alterationBAC aCGHProbe signal intensity
nssv3008371sequence alterationBAC aCGHProbe signal intensity
nssv3008731sequence alterationBAC aCGHProbe signal intensity
nssv3008856sequence alterationBAC aCGHProbe signal intensity
nssv3009433sequence alterationBAC aCGHProbe signal intensity
nssv3009579sequence alterationBAC aCGHProbe signal intensity
nssv3009884sequence alterationBAC aCGHProbe signal intensity
nssv3010016sequence alterationBAC aCGHProbe signal intensity
nssv3010225sequence alterationBAC aCGHProbe signal intensity
nssv3010253sequence alterationBAC aCGHProbe signal intensity
nssv3010263sequence alterationBAC aCGHProbe signal intensity
nssv3010449sequence alterationBAC aCGHProbe signal intensity
nssv3010713sequence alterationBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv3006781RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3006886RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3006916RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3007700RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3007790RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3007856RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3007911RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3008198RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3008371RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3008731RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3008856RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3009433RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3009579RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3009884RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3010016RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3010225RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3010253RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3010263RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3010449RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3010713RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8392,250571,073
nssv3006781RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3006886RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3006916RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3007700RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3007790RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3007856RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3007911RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3008198RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3008371RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3008731RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3008856RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3009433RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3009579RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3009884RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3010016RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3010225RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3010253RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3010263RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3010449RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3010713RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8342,250521,073
nssv3006781Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3006886Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3006916Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3007700Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3007790Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3007856Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3007911Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3008198Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3008371Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3008731Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3008856Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3009433Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3009579Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3009884Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3010016Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3010225Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3010253Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3010263Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3010449Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073
nssv3010713Submitted genomicNCBI34 (hg16)NC_000008.8Chr8332,250511,073

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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