U.S. flag

An official website of the United States government

nsv5404988

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 19 studies. See in: genome view    
Submitted genomic160,353,751-160,353,794Question Mark
Overlapping variant regions from other studies: 112 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):160,323,541-160,323,584Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5404988Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1160,353,751160,353,794
nsv5404988RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,323,541160,323,584

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16891072alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16891072Submitted genomicNC_000001.11:g.160
353751_160353794in
s281
GRCh38 (hg38)NC_000001.11Chr1160,353,751160,353,794
nssv16891072RemappedPerfectNC_000001.10:g.160
323541_160323584in
s281
GRCh37.p13First PassNC_000001.10Chr1160,323,541160,323,584

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)
nssv16891072<0.00116404
Support Center