U.S. flag

An official website of the United States government

nsv5423183

  • 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: 186 SVs from 30 studies. See in: genome view    
Submitted genomic15,854,985-15,855,036Question Mark
Overlapping variant regions from other studies: 186 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):17,227,304-17,227,355Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423183Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2115,854,98515,855,036
nsv5423183RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2117,227,30417,227,355

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17734119alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17734119Submitted genomicNC_000021.9:g.1585
4985_15855036ins27
9
GRCh38 (hg38)NC_000021.9Chr2115,854,98515,855,036
nssv17734119RemappedPerfectNC_000021.8:g.1722
7304_17227355ins27
9
GRCh37.p13First PassNC_000021.8Chr2117,227,30417,227,355

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)
nssv17734119<0.00116404
Support Center