A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607713



Internal ID16395122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84546973..84694195hg38UCSC Ensembl
Innerchr7:84176289..84323511hg19UCSC Ensembl
Innerchr7:84014225..84161447hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38147223
hg19147223
hg18147223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11488n54
Supporting Variantsnssv1089374
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607713
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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