A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094545



Internal ID15947731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:133776473..133935221hg38UCSC Ensembl
Innerchr7:133461226..133619974hg19UCSC Ensembl
Innerchr7:133111766..133270514hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38158749
hg19158749
hg18158749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608443
Supporting Variants
Samples
Known GenesEXOC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094545
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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