A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939357



Internal ID16233313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:38377270..38385327hg38UCSC Ensembl
Innerchr20:37005912..37013969hg19UCSC Ensembl
Innerchr20:36439326..36447383hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg388058
hg198058
hg188058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585965
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)nssv939357
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