A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063034



Internal ID18805565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59862589..59943263hg38UCSC Ensembl
Innerchr20:58437644..58518318hg19UCSC Ensembl
Innerchr20:57871039..57951713hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3880675
hg1980675
hg1880675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4336n100
Supporting Variantsnssv3584283
Samples
Known GenesFAM217B, PPP1R3D, SYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063034
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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