A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1087865



Internal ID15941051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75731521..75771091hg38UCSC Ensembl
Innerchr7:75360839..75400409hg19UCSC Ensembl
Innerchr7:75198775..75238345hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3839571
hg1939571
hg1839571
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607516
Supporting Variants
Samples
Known GenesCCL26, HIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1087865
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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