A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1084766



Internal ID15591266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57091428..57503955hg38UCSC Ensembl
Innerchr7:57159135..57563661hg19UCSC Ensembl
Innerchr7:57163077..57567603hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38412528
hg19404527
hg18404527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607046
Supporting Variants
Samples
Known GenesGUSBP10, MIR3147, ZNF479, ZNF716
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1084766
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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