A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605928



Internal ID16393337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3614948..3625408hg38UCSC Ensembl
Innerchr7:3654580..3665040hg19UCSC Ensembl
Innerchr7:3621106..3631566hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3810461
hg1910461
hg1810461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078610
Samples
Known GenesSDK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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