A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156178



Internal ID15854613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136839412hg38UCSC Ensembl
Innerchr8:137687955..137851655hg19UCSC Ensembl
Innerchr8:137757137..137920837hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38163701
hg19163701
hg18163701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612402
Supporting Variants
Samples1780862227_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156178
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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