A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156155



Internal ID15874630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675295..136834761hg38UCSC Ensembl
Innerchr8:137687538..137847004hg19UCSC Ensembl
Innerchr8:137756720..137916186hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38159467
hg19159467
hg18159467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612386
Supporting Variants
SamplesHGDP00564
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156155
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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