A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938913



Internal ID16232869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:21936755..21968955hg38UCSC Ensembl
Innerchr20:21917393..21949593hg19UCSC Ensembl
Innerchr20:21865393..21897593hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3832201
hg1932201
hg1832201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585717
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)nssv938913
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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