A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv944155



Internal ID16238111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64055664..64120101hg38UCSC Ensembl
Innerchr20:62687017..62751454hg19UCSC Ensembl
Innerchr20:62157461..62221898hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3864438
hg1964438
hg1864438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586730
Supporting Variants
Samples
Known GenesC20orf201, MIR6813, NPBWR2, OPRL1, RGS19, TCEA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv944155
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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