A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602921



Internal ID16390330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35534425..35587406hg38UCSC Ensembl
Innerchr6:35502202..35555183hg19UCSC Ensembl
Innerchr6:35610180..35663161hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3852982
hg1952982
hg1852982
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10626n54
Supporting Variantsnssv1058209, nssv1154300
SamplesHGDP01262
Known GenesFKBP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602921
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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