A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937568



Internal ID16231524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:6141205..6149378hg38UCSC Ensembl
Innerchr20:6121852..6130025hg19UCSC Ensembl
Innerchr20:6069852..6078025hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg388174
hg198174
hg188174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585350
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)nssv937568
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer