A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1122276



Internal ID15975462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136838205hg38UCSC Ensembl
Innerchr8:137687955..137850448hg19UCSC Ensembl
Innerchr8:137757137..137919630hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38162494
hg19162494
hg18162494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612401
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)nssv1122276
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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