A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605720



Internal ID16046443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:977312..1121522hg38UCSC Ensembl
Innerchr7:1016948..1161158hg19UCSC Ensembl
Innerchr7:983474..1127684hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38144211
hg19144211
hg18144211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077832
Samples
Known GenesC7orf50, CYP2W1, GPER1, GPR146, MIR339
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605720
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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