A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586226



Internal ID16373635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53858408..53859343hg38UCSC Ensembl
Innerchr20:52474947..52475882hg19UCSC Ensembl
Innerchr20:51908354..51909289hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38936
hg19936
hg18936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7606n54
Supporting Variantsnssv941224
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586226
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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