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nsv6293833

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,668

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 160 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):29,861,894-29,869,561Question Mark
Overlapping variant regions from other studies: 160 SVs from 41 studies. See in: genome view    
Submitted genomic30,014,827-30,022,494Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6293833RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1229,861,89429,869,561
nsv6293833Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1230,014,82730,022,494

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17658367alu insertionCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17658367RemappedPerfectNC_000012.12:g.298
61894_29869561ins?
GRCh38.p12First PassNC_000012.12Chr1229,861,89429,869,561
nssv17658367Submitted genomicNC_000012.11:g.300
14827_30022494ins?
GRCh37 (hg19)NC_000012.11Chr1230,014,82730,022,494

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv176583670.49331586404
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