A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156363



Internal ID15877281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22106867..22158340hg38UCSC Ensembl
Innerchr8:21964378..22015853hg19UCSC Ensembl
Innerchr8:22020323..22071798hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3851474
hg1951476
hg1851476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610769
Supporting Variants
SamplesHGDP00961
Known GenesHR, LGI3, NUDT18, REEP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156363
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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