A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941914



Internal ID15889184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61252123..61257735hg38UCSC Ensembl
Innerchr20:59827179..59832791hg19UCSC Ensembl
Innerchr20:59260574..59266186hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385613
hg195613
hg185613
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586415
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)nssv941914
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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