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nsv5446095

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:320

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 129 SVs from 19 studies. See in: genome view    
Submitted genomic171,977,538-171,977,857Question Mark
Overlapping variant regions from other studies: 129 SVs from 19 studies. See in: genome view    
Remapped(Score: Pass):172,842,477-172,842,766Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5446095Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2171,977,538171,977,857
nsv5446095RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2172,842,477172,842,766

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16922504deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16922504Submitted genomicNC_000002.12:g.171
977538_171977857de
l
GRCh38 (hg38)NC_000002.12Chr2171,977,538171,977,857
nssv16922504RemappedPassNC_000002.11:g.172
842477_172842766de
l
GRCh37.p13First PassNC_000002.11Chr2172,842,477172,842,766

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)
nssv16922504<0.00156404
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