A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1087864



Internal ID15941050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75731521..75758619hg38UCSC Ensembl
Innerchr7:75360839..75387937hg19UCSC Ensembl
Innerchr7:75198775..75225873hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3827099
hg1927099
hg1827099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607515
Supporting Variants
Samples
Known GenesHIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1087864
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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