A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061458



Internal ID19150677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61541731..61670752hg38UCSC Ensembl
Innerchr20:60116787..60245808hg19UCSC Ensembl
Innerchr20:59550182..59679203hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38129022
hg19129022
hg18129022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584454
Samples
Known GenesCDH4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061458
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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