A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611976



Internal ID16399385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114248905..115211636hg38UCSC Ensembl
Innerchr8:115261134..116223865hg19UCSC Ensembl
Innerchr8:115330310..116293041hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38962732
hg19962732
hg18962732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1119765
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611976
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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