A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611567



Internal ID16398976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77475007..77539986hg38UCSC Ensembl
Innerchr8:78387243..78452222hg19UCSC Ensembl
Innerchr8:78549798..78614777hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3864980
hg1964980
hg1864980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117008
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611567
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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