A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609716



Internal ID16397125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:3029910..3033287hg38UCSC Ensembl
Innerchr8:2887432..2890809hg19UCSC Ensembl
Innerchr8:2874839..2878216hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg383378
hg193378
hg183378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11855n54
Supporting Variantsnssv1104045
Samples
Known GenesCSMD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609716
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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