A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941933



Internal ID16235889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61252182..61253373hg38UCSC Ensembl
Innerchr20:59827238..59828429hg19UCSC Ensembl
Innerchr20:59260633..59261824hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381192
hg191192
hg181192
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586420
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)nssv941933
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer