A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059132



Internal ID18801663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59845169..59928674hg38UCSC Ensembl
Innerchr20:58420224..58503729hg19UCSC Ensembl
Innerchr20:57853619..57937124hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3883506
hg1983506
hg1883506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4335n100
Supporting Variantsnssv3584258
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)nsv1059132
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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