A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067145



Internal ID18809676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57481818..57523849hg38UCSC Ensembl
Innerchr19:57993186..58035217hg19UCSC Ensembl
Innerchr19:62684998..62727029hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3842032
hg1942032
hg1842032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570454
Samples
Known GenesZNF419, ZNF773
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067145
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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