A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612696



Internal ID16400105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142308160..142335051hg38UCSC Ensembl
Innerchr8:143389521..143416412hg19UCSC Ensembl
Innerchr8:143387428..143414319hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3826892
hg1926892
hg1826892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12394n54
Supporting Variantsnssv1124914
Samples
Known GenesTSNARE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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