A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941885



Internal ID15889155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61252058..61253165hg38UCSC Ensembl
Innerchr20:59827114..59828221hg19UCSC Ensembl
Innerchr20:59260509..59261616hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381108
hg191108
hg181108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586405
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)nssv941885
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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