U.S. flag

An official website of the United States government

nsv5523856

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,531

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 179 SVs from 38 studies. See in: genome view    
Submitted genomic48,891,163-48,916,693Question Mark
Overlapping variant regions from other studies: 179 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):49,394,420-49,419,950Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523856Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,891,16348,916,693
nsv5523856RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,394,42049,419,950

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723930deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723930Submitted genomicNC_000019.10:g.488
91163_48916693del
GRCh38 (hg38)NC_000019.10Chr1948,891,16348,916,693
nssv17723930RemappedPerfectNC_000019.9:g.4939
4420_49419950del
GRCh37.p13First PassNC_000019.9Chr1949,394,42049,419,950

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)
nssv17723930<0.00116404
Support Center