A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065779



Internal ID19154998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12409110..12438841hg38UCSC Ensembl
Innerchr19:12519924..12549655hg19UCSC Ensembl
Innerchr19:12380924..12410655hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3829732
hg1929732
hg1829732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3434n100
Supporting Variantsnssv3564758
Samples
Known GenesZNF443
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065779
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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