A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586280



Internal ID16373689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54102016..54141877hg38UCSC Ensembl
Innerchr20:52718555..52758416hg19UCSC Ensembl
Innerchr20:52151962..52191823hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3839862
hg1939862
hg1839862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941571
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586280
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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