A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156622



Internal ID15879851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83242979..83343029hg38UCSC Ensembl
Innerchr8:84155214..84255264hg19UCSC Ensembl
Innerchr8:84317769..84417819hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38100051
hg19100051
hg18100051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611633
Supporting Variants
SamplesNINDS_116
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156622
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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