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nsv5485568

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:88,974

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1302 SVs from 97 studies. See in: genome view    
Submitted genomic38,269,535-38,358,508Question Mark
Overlapping variant regions from other studies: 1302 SVs from 97 studies. See in: genome view    
Remapped(Score: Perfect):38,309,136-38,398,109Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5485568Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr738,269,53538,358,508
nsv5485568RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr738,309,13638,398,109

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16996227deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16996227Submitted genomicNC_000007.14:g.382
69535_38358508del
GRCh38 (hg38)NC_000007.14Chr738,269,53538,358,508
nssv16996227RemappedPerfectNC_000007.13:g.383
09136_38398109del
GRCh37.p13First PassNC_000007.13Chr738,309,13638,398,109

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16996227<0.00156404
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