A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569788



Internal ID18868069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19695577..19758523hg38UCSC Ensembl
Innerchr19:19806386..19869332hg19UCSC Ensembl
Innerchr19:19667386..19730332hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3862947
hg1962947
hg1862947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062212
Supporting Variants
Samples
Known GenesLINC00663, ZNF14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3569788
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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