A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586414



Internal ID16373823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61252123..61253373hg38UCSC Ensembl
Innerchr20:59827179..59828429hg19UCSC Ensembl
Innerchr20:59260574..59261824hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381251
hg191251
hg181251
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7639n54
Supporting Variantsnssv941907, nssv941911, nssv941913, nssv941910, nssv941909, nssv941908, nssv941912, nssv941906
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586414
Frequency
Sample Size17421
Observed Gain7
Observed Loss1
Observed Complex0
Frequencyn/a


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