A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585324



Internal ID16372733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5039591..5078323hg38UCSC Ensembl
Innerchr20:5020237..5058969hg19UCSC Ensembl
Innerchr20:4968237..5006969hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3838733
hg1938733
hg1838733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937453
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585324
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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