A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611760



Internal ID16399169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95416220..95594800hg38UCSC Ensembl
Innerchr8:96428448..96607028hg19UCSC Ensembl
Innerchr8:96497624..96676204hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38178581
hg19178581
hg18178581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117859
Samples
Known GenesLOC100616530
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611760
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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