A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605939



Internal ID16046662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3915884..4573976hg38UCSC Ensembl
Innerchr7:3955516..4613607hg19UCSC Ensembl
Innerchr7:3922042..4580133hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38658093
hg19658092
hg18658092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155132, nssv1155128, nssv1155129, nssv1155131, nssv1155127, nssv1155130
SamplesHGDP01001, HGDP01014, HGDP01016, HGDP01003, HGDP01017, HGDP01018
Known GenesSDK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605939
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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