A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612356



Internal ID16399765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136188762..136328039hg38UCSC Ensembl
Innerchr8:137201005..137340282hg19UCSC Ensembl
Innerchr8:137270187..137409464hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38139278
hg19139278
hg18139278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1122182
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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