A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611577



Internal ID16052300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78770378..79192705hg38UCSC Ensembl
Innerchr8:79682613..80104940hg19UCSC Ensembl
Innerchr8:79845168..80267495hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38422328
hg19422328
hg18422328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117019
Samples
Known GenesIL7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611577
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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