A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937567



Internal ID16231523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:6141205..6148621hg38UCSC Ensembl
Innerchr20:6121852..6129268hg19UCSC Ensembl
Innerchr20:6069852..6077268hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg387417
hg197417
hg187417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585349
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)nssv937567
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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