A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586584



Internal ID16373993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63597719..63609933hg38UCSC Ensembl
Innerchr20:62229072..62241286hg19UCSC Ensembl
Innerchr20:61699516..61711730hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3812215
hg1912215
hg1812215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7670n54
Supporting Variantsnssv943763
Samples
Known GenesGMEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586584
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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