A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612689



Internal ID16400098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142122305..142153562hg38UCSC Ensembl
Innerchr8:143203666..143234923hg19UCSC Ensembl
Innerchr8:143201573..143232830hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3831258
hg1931258
hg1831258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1124910
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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