U.S. flag

An official website of the United States government

nsv5409404

  • 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: 129 SVs from 16 studies. See in: genome view    
Submitted genomic200,438,728-200,438,779Question Mark
Overlapping variant regions from other studies: 129 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):201,303,451-201,303,502Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5409404Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2200,438,728200,438,779
nsv5409404RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2201,303,451201,303,502

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16922830alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16922830Submitted genomicNC_000002.12:g.200
438728_200438779in
s280
GRCh38 (hg38)NC_000002.12Chr2200,438,728200,438,779
nssv16922830RemappedPerfectNC_000002.11:g.201
303451_201303502in
s280
GRCh37.p13First PassNC_000002.11Chr2201,303,451201,303,502

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)
nssv16922830<0.00116404
Support Center