A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661897



Internal ID18960178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62617247..63273371hg38UCSC Ensembl
Innerchr7:62077625..62733749hg19UCSC Ensembl
Innerchr7:61715060..62371184hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38656125
hg19656125
hg18656125
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032212
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661897
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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