A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526599



Internal ID15453892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42528756..42604069hg38UCSC Ensembl
Innerchr6:42496494..42571807hg19UCSC Ensembl
Innerchr6:42604472..42679785hg18UCSC Ensembl
Innerchr6:42604472..42679785hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3875314
hg1975314
hg1875314
hg1775314
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702918
Samples
Known GenesUBR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526599
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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