A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586695



Internal ID16374104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63928611..63965638hg38UCSC Ensembl
Innerchr20:62559964..62596991hg19UCSC Ensembl
Innerchr20:62030408..62067435hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3837028
hg1937028
hg1837028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944021
Samples
Known GenesDNAJC5, MIR1914, MIR647, UCKL1, UCKL1-AS1, ZNF512B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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