A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063954



Internal ID19153173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20817756..20994771hg38UCSC Ensembl
Innerchr19:21000562..21177577hg19UCSC Ensembl
Innerchr19:20792402..20969417hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38177016
hg19177016
hg18177016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570575
Samples
Known GenesZNF85
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063954
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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