A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655547



Internal ID18953828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65176738..65607180hg38UCSC Ensembl
Innerchr7:64637116..65072093hg19UCSC Ensembl
Innerchr7:64274551..64709528hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38430443
hg19434978
hg18434978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027826
Supporting Variants
Samples
Known GenesZNF92
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655547
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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