A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662073



Internal ID18613668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119385956..120677299hg38UCSC Ensembl
Innerchr7:119026010..120317353hg19UCSC Ensembl
Innerchr7:118813246..120104589hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg381291344
hg191291344
hg181291344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031971
Supporting Variants
Samples
Known GenesKCND2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662073
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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