A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1085694



Internal ID15938880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:67665262..67667091hg38UCSC Ensembl
Innerchr7:67130249..67132078hg19UCSC Ensembl
Innerchr7:66767684..66769513hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381830
hg191830
hg181830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607424
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)nssv1085694
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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