A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612329



Internal ID16399738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133612305..133637162hg38UCSC Ensembl
Innerchr8:134624548..134649405hg19UCSC Ensembl
Innerchr8:134693730..134718587hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3824858
hg1924858
hg1824858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1121520, nssv1121521, nssv1121519
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612329
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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