A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586405



Internal ID16027128
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 StatusM
Merged Variantsdgv7636n54
Supporting Variantsnssv941881, nssv941882, nssv941883, nssv941885, nssv941884, nssv941880
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586405
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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