A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1082641



Internal ID15935827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31551087..31553119hg38UCSC Ensembl
Innerchr7:31590701..31592733hg19UCSC Ensembl
Innerchr7:31557226..31559258hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg382033
hg192033
hg182033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606581
Supporting Variants
Samples
Known GenesCCDC129
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1082641
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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