A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066818



Internal ID19156037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:12748753..12800886hg38UCSC Ensembl
Innerchr20:12729400..12781534hg19UCSC Ensembl
Innerchr20:12677400..12729534hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3852134
hg1952135
hg1852135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4246n100
Supporting Variantsnssv3599391
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)nsv1066818
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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