A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662110



Internal ID18960391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:120996742..121032450hg38UCSC Ensembl
Innerchr7:120636796..120672504hg19UCSC Ensembl
Innerchr7:120424032..120459740hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3835709
hg1935709
hg1835709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030988
Supporting Variants
Samples
Known GenesCPED1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662110
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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