U.S. flag

An official website of the United States government

nsv5411212

  • 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: 206 SVs from 23 studies. See in: genome view    
Submitted genomic17,107,542-17,107,593Question Mark
Overlapping variant regions from other studies: 206 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):16,965,051-16,965,102Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5411212Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr817,107,54217,107,593
nsv5411212RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr816,965,05116,965,102

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17008892alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17008892Submitted genomicNC_000008.11:g.171
07542_17107593ins2
80
GRCh38 (hg38)NC_000008.11Chr817,107,54217,107,593
nssv17008892RemappedPerfectNC_000008.10:g.169
65051_16965102ins2
80
GRCh37.p13First PassNC_000008.10Chr816,965,05116,965,102

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)
nssv17008892<0.00126404
Support Center