A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610179



Internal ID16397588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8613838..8643812hg38UCSC Ensembl
Innerchr8:8471348..8501322hg19UCSC Ensembl
Innerchr8:8508758..8538732hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3829975
hg1929975
hg1829975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105936
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610179
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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