A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662065



Internal ID18960346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:118486165..118521306hg38UCSC Ensembl
Innerchr7:118126219..118161360hg19UCSC Ensembl
Innerchr7:117913455..117948596hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3835142
hg1935142
hg1835142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024124
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)nssv3662065
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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