A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611747



Internal ID16399156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:93130978..93155425hg38UCSC Ensembl
Innerchr8:94143207..94167654hg19UCSC Ensembl
Innerchr8:94212383..94236830hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3824448
hg1924448
hg1824448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156632
Samples1780854017_A
Known GenesC8orf87
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611747
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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