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nsv5446549

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:41,651

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 309 SVs from 51 studies. See in: genome view    
Submitted genomic127,170,686-127,212,336Question Mark
Overlapping variant regions from other studies: 309 SVs from 51 studies. See in: genome view    
Remapped(Score: Perfect):127,928,262-127,969,912Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5446549Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2127,170,686127,212,336
nsv5446549RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2127,928,262127,969,912

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16917734duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16917734Submitted genomicNC_000002.12:g.127
170686_127212336du
p
GRCh38 (hg38)NC_000002.12Chr2127,170,686127,212,336
nssv16917734RemappedPerfectNC_000002.11:g.127
928262_127969912du
p
GRCh37.p13First PassNC_000002.11Chr2127,928,262127,969,912

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)
nssv16917734<0.00116404
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