A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612968



Internal ID16400377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144699331..144700762hg38UCSC Ensembl
Innerchr8:145924716..145926147hg19UCSC Ensembl
Innerchr8:145895525..145896956hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381432
hg191432
hg181432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1125831
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612968
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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