A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586401



Internal ID16027124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61252058..61252784hg38UCSC Ensembl
Innerchr20:59827114..59827840hg19UCSC Ensembl
Innerchr20:59260509..59261235hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38727
hg19727
hg18727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7635n54
Supporting Variantsnssv941872
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586401
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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