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nsv5422676

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:159

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 128 SVs from 24 studies. See in: genome view    
Submitted genomic44,342,777-44,342,935Question Mark
Overlapping variant regions from other studies: 128 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):44,808,449-44,808,607Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5422676Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr144,342,77744,342,935
nsv5422676RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr144,808,44944,808,607

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902563deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902563Submitted genomicNC_000001.11:g.443
42777_44342935del
GRCh38 (hg38)NC_000001.11Chr144,342,77744,342,935
nssv16902563RemappedPerfectNC_000001.10:g.448
08449_44808607del
GRCh37.p13First PassNC_000001.10Chr144,808,44944,808,607

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)
nssv16902563<0.00126404
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