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nsv499487

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44,611

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 623 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):247,127,704-247,172,314Question Mark
Overlapping variant regions from other studies: 628 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):247,291,006-247,335,616Question Mark
Overlapping variant regions from other studies: 284 SVs from 22 studies. See in: genome view    
Submitted genomic245,357,629-245,402,239Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv499487RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1247,127,704247,172,314
nsv499487RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1247,291,006247,335,616
nsv499487Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000001.9Chr1245,357,629245,402,239

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv585490inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv585490RemappedPerfectNC_000001.11:g.247
127704_247172314in
v
GRCh38.p12First PassNC_000001.11Chr1247,127,704247,172,314
nssv585490RemappedPerfectNC_000001.10:g.247
291006_247335616in
v
GRCh37.p13First PassNC_000001.10Chr1247,291,006247,335,616
nssv585490Submitted genomicNC_000001.9:g.2453
57629_245402239inv
NCBI36 (hg18)NC_000001.9Chr1245,357,629245,402,239

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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