A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937453



Internal ID16231409
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 StatusS
Merged Variantsnsv585324
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv937453
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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