A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156190



Internal ID15875017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675987..136838260hg38UCSC Ensembl
Innerchr8:137688230..137850503hg19UCSC Ensembl
Innerchr8:137757412..137919685hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38162274
hg19162274
hg18162274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612420
Supporting Variants
SamplesHGDP00622
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156190
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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