A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611902



Internal ID16399311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:111312835..111699809hg38UCSC Ensembl
Innerchr8:112325064..112712038hg19UCSC Ensembl
Innerchr8:112394240..112781214hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38386975
hg19386975
hg18386975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156372
Samples1780862360_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611902
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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