A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062212



Internal ID19151431
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 StatusM
Merged Variantsdgv3455n100
Supporting Variantsnssv3569788
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)nsv1062212
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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