A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057192



Internal ID18799723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:36514051..36839310hg38UCSC Ensembl
Innerchr20:35142454..35467713hg19UCSC Ensembl
Innerchr20:34575868..34901127hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38325260
hg19325260
hg18325260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584755
Samples
Known GenesC20orf24, DLGAP4, DSN1, MYL9, NDRG3, SLA2, SOGA1, TGIF2, TGIF2-C20orf24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057192
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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