A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602922



Internal ID16390331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35534425..35594863hg38UCSC Ensembl
Innerchr6:35502202..35562640hg19UCSC Ensembl
Innerchr6:35610180..35670618hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3860439
hg1960439
hg1860439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10626n54
Supporting Variantsnssv1154302, nssv1154301
SamplesHGDP00479, HGDP00941
Known GenesFKBP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602922
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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