A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611751



Internal ID16052474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94709207..94730166hg38UCSC Ensembl
Innerchr8:95721435..95742394hg19UCSC Ensembl
Innerchr8:95790611..95811570hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3820960
hg1920960
hg1820960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117844
Samples
Known GenesDPY19L4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611751
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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