A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662213



Internal ID18960494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:133627482..133695129hg38UCSC Ensembl
Innerchr7:133312235..133379882hg19UCSC Ensembl
Innerchr7:132962775..133030422hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3867648
hg1967648
hg1867648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018425
Supporting Variants
Samples
Known GenesEXOC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662213
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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