A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586605



Internal ID16374014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63608014..63620691hg38UCSC Ensembl
Innerchr20:62239367..62252044hg19UCSC Ensembl
Innerchr20:61709811..61722488hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3812678
hg1912678
hg1812678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv943825
Samples
Known GenesGMEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586605
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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