A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585727



Internal ID16026450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23750775..23827687hg38UCSC Ensembl
Innerchr20:23731412..23808324hg19UCSC Ensembl
Innerchr20:23679412..23756324hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3876913
hg1976913
hg1876913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152375
Samples1780854017_A
Known GenesCST1, CST2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585727
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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