A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610862



Internal ID16051585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:26566664..26587153hg38UCSC Ensembl
Innerchr8:26424180..26444669hg19UCSC Ensembl
Innerchr8:26480097..26500586hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3820490
hg1920490
hg1820490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1109352
Samples
Known GenesDPYSL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610862
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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