A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062840



Internal ID18805371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59845169..59925649hg38UCSC Ensembl
Innerchr20:58420224..58500704hg19UCSC Ensembl
Innerchr20:57853619..57934099hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3880481
hg1980481
hg1880481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4335n100
Supporting Variantsnssv3584257
Samples
Known GenesPHACTR3, SYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062840
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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