A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586400



Internal ID16373809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61128958..61149665hg38UCSC Ensembl
Innerchr20:59704014..59724721hg19UCSC Ensembl
Innerchr20:59137409..59158116hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3820708
hg1920708
hg1820708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151398
SamplesHGDP01049
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586400
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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