A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586351



Internal ID16373760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58583589..58617746hg38UCSC Ensembl
Innerchr20:57158645..57192802hg19UCSC Ensembl
Innerchr20:56592051..56626208hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3834158
hg1934158
hg1834158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941795
Samples
Known GenesAPCDD1L-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586351
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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