A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661779



Internal ID18960060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62506780..62909444hg38UCSC Ensembl
Innerchr7:61888128..62369822hg19UCSC Ensembl
Innerchr7:61525563..62007257hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38402665
hg19481695
hg18481695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035060
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)nssv3661779
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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