A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585746



Internal ID16026469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25090818..25489420hg38UCSC Ensembl
Innerchr20:25071454..25470056hg19UCSC Ensembl
Innerchr20:25019454..25418056hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38398603
hg19398603
hg18398603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938973
Samples
Known GenesABHD12, ENTPD6, GINS1, LOC284798, NINL, PYGB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585746
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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