U.S. flag

An official website of the United States government

nsv5403120

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 22 studies. See in: genome view    
Submitted genomic157,041,701-157,041,752Question Mark
Overlapping variant regions from other studies: 111 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):157,011,493-157,011,544Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5403120Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1157,041,701157,041,752
nsv5403120RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1157,011,493157,011,544

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890947alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890947Submitted genomicNC_000001.11:g.157
041701_157041752in
s280
GRCh38 (hg38)NC_000001.11Chr1157,041,701157,041,752
nssv16890947RemappedPerfectNC_000001.10:g.157
011493_157011544in
s280
GRCh37.p13First PassNC_000001.10Chr1157,011,493157,011,544

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)
nssv16890947<0.00116404
Support Center