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nsv5411541

  • 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: 110 SVs from 13 studies. See in: genome view    
Submitted genomic171,385,382-171,385,433Question Mark
Overlapping variant regions from other studies: 110 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):172,241,892-172,241,943Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5411541Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2171,385,382171,385,433
nsv5411541RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2172,241,892172,241,943

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16926842alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16926842Submitted genomicNC_000002.12:g.171
385382_171385433in
s237
GRCh38 (hg38)NC_000002.12Chr2171,385,382171,385,433
nssv16926842RemappedPerfectNC_000002.11:g.172
241892_172241943in
s237
GRCh37.p13First PassNC_000002.11Chr2172,241,892172,241,943

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)
nssv16926842<0.00126404
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