A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585283



Internal ID16372692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3699633..3720485hg38UCSC Ensembl
Innerchr20:3680280..3701132hg19UCSC Ensembl
Innerchr20:3628280..3649132hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3820853
hg1920853
hg1820853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152354
SamplesHGDP00451
Known GenesSIGLEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585283
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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