A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156151



Internal ID15874599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136280918..136309563hg38UCSC Ensembl
Innerchr8:137293161..137321806hg19UCSC Ensembl
Innerchr8:137362343..137390988hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3828646
hg1928646
hg1828646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612357
Supporting Variants
SamplesHGDP00559
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156151
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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