A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607801



Internal ID16395210
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 StatusM
Merged Variants
Supporting Variantsnssv1090180
Samples
Known GenesCCDC132
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607801
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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