A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065960



Internal ID18808491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20659865..20798323hg38UCSC Ensembl
Innerchr19:20842671..20981129hg19UCSC Ensembl
Innerchr19:20634511..20772969hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38138459
hg19138459
hg18138459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3467n100
Supporting Variantsnssv3724322
Samples
Known GenesZNF626
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065960
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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