U.S. flag

An official website of the United States government

nsv5529360

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,158

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 140 SVs from 27 studies. See in: genome view    
Submitted genomic36,520,640-36,521,797Question Mark
Overlapping variant regions from other studies: 140 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):37,011,542-37,012,699Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5529360Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,520,64036,521,797
nsv5529360RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1937,011,54237,012,699

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723108deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723108Submitted genomicNC_000019.10:g.365
20640_36521797del
GRCh38 (hg38)NC_000019.10Chr1936,520,64036,521,797
nssv17723108RemappedPerfectNC_000019.9:g.3701
1542_37012699del
GRCh37.p13First PassNC_000019.9Chr1937,011,54237,012,699

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)
nssv17723108<0.00116404
Support Center