A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661976



Internal ID18960257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64150329..64442877hg38UCSC Ensembl
Innerchr7:63610707..63903255hg19UCSC Ensembl
Innerchr7:63248142..63540690hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38292549
hg19292549
hg18292549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018858
Supporting Variants
Samples
Known GenesYWHAEP1, ZNF679, ZNF735, ZNF736
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661976
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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