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nsv5531093

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,020

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 151 SVs from 26 studies. See in: genome view    
Submitted genomic39,530,314-39,535,333Question Mark
Overlapping variant regions from other studies: 151 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):40,020,954-40,025,973Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5531093Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1939,530,31439,535,333
nsv5531093RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1940,020,95440,025,973

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723343deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723343Submitted genomicNC_000019.10:g.395
30314_39535333del
GRCh38 (hg38)NC_000019.10Chr1939,530,31439,535,333
nssv17723343RemappedPerfectNC_000019.9:g.4002
0954_40025973del
GRCh37.p13First PassNC_000019.9Chr1940,020,95440,025,973

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)
nssv17723343<0.00116404
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