A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612688



Internal ID16400097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142103210..142151951hg38UCSC Ensembl
Innerchr8:143184571..143233312hg19UCSC Ensembl
Innerchr8:143182478..143231219hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3848742
hg1948742
hg1848742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1124909
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612688
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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