A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610822



Internal ID16051545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25172277..25216845hg38UCSC Ensembl
Innerchr8:25029792..25074361hg19UCSC Ensembl
Innerchr8:25085709..25130278hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3844569
hg1944570
hg1844570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107861
Samples
Known GenesDOCK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610822
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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