A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611311



Internal ID16398720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:49952670..50067760hg38UCSC Ensembl
Innerchr8:50865230..50980320hg19UCSC Ensembl
Innerchr8:51027783..51142873hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38115091
hg19115091
hg18115091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115122
Samples
Known GenesSNTG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611311
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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