U.S. flag

An official website of the United States government

nsv5431501

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:82

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 154 SVs from 23 studies. See in: genome view    
Submitted genomic171,506,526-171,506,607Question Mark
Overlapping variant regions from other studies: 157 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):171,475,665-171,475,746Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5431501Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1171,506,526171,506,607
nsv5431501RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1171,475,665171,475,746

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892246deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892246Submitted genomicNC_000001.11:g.171
506526_171506607de
l
GRCh38 (hg38)NC_000001.11Chr1171,506,526171,506,607
nssv16892246RemappedPerfectNC_000001.10:g.171
475665_171475746de
l
GRCh37.p13First PassNC_000001.10Chr1171,475,665171,475,746

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)
nssv16892246<0.00126404
Support Center