A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156193



Internal ID15856016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675987..136839412hg38UCSC Ensembl
Innerchr8:137688230..137851655hg19UCSC Ensembl
Innerchr8:137757412..137920837hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38163426
hg19163426
hg18163426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612421
Supporting Variants
Samples1798860361_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156193
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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