A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063442



Internal ID19152661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53783980..53811681hg38UCSC Ensembl
Innerchr20:52400519..52428220hg19UCSC Ensembl
Innerchr20:51833926..51861627hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3827702
hg1927702
hg1827702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4325n100
Supporting Variantsnssv3586083
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063442
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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