A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1122216



Internal ID15975402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136670241..136843835hg38UCSC Ensembl
Innerchr8:137682484..137856078hg19UCSC Ensembl
Innerchr8:137751666..137925260hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38173595
hg19173595
hg18173595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612378
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1122216
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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