A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1090180



Internal ID15943366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:93228492..93260436hg38UCSC Ensembl
Innerchr7:92857805..92889748hg19UCSC Ensembl
Innerchr7:92695741..92727684hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3831945
hg1931944
hg1831944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607801
Supporting Variants
Samples
Known GenesCCDC132
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1090180
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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