A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1122366



Internal ID15975552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675987..136833690hg38UCSC Ensembl
Innerchr8:137688230..137845933hg19UCSC Ensembl
Innerchr8:137757412..137915115hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38157704
hg19157704
hg18157704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612417
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)nssv1122366
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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