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nsv5536321

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 110 SVs from 12 studies. See in: genome view    
Submitted genomic171,360,533-171,360,538Question Mark
Overlapping variant regions from other studies: 110 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):172,217,043-172,217,048Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5536321Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2171,360,533171,360,538
nsv5536321RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2172,217,043172,217,048

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16926835insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16926835Submitted genomicNC_000002.12:g.171
360533_171360538in
s67
GRCh38 (hg38)NC_000002.12Chr2171,360,533171,360,538
nssv16926835RemappedPerfectNC_000002.11:g.172
217043_172217048in
s67
GRCh37.p13First PassNC_000002.11Chr2172,217,043172,217,048

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)
nssv16926835<0.00116404
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