A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586212



Internal ID16373621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53667312..53674942hg38UCSC Ensembl
Innerchr20:52283851..52291481hg19UCSC Ensembl
Innerchr20:51717258..51724888hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg387631
hg197631
hg187631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7603n54
Supporting Variantsnssv941158
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586212
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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