A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063895



Internal ID19153114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23734421..23811022hg38UCSC Ensembl
Innerchr20:23715058..23791659hg19UCSC Ensembl
Innerchr20:23663058..23739659hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3876602
hg1976602
hg1876602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4287n100
Supporting Variantsnssv3584668
Samples
Known GenesCST1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063895
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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