A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941899



Internal ID15889169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61252123..61252839hg38UCSC Ensembl
Innerchr20:59827179..59827895hg19UCSC Ensembl
Innerchr20:59260574..59261290hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38717
hg19717
hg18717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586409
Supporting Variants
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv941899
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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