A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1084680



Internal ID15591180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55216561..55241732hg38UCSC Ensembl
Innerchr7:55284254..55309425hg19UCSC Ensembl
Innerchr7:55251748..55276919hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3825172
hg1925172
hg1825172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607032
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1084680
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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