A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059474



Internal ID19148693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12405336..12434058hg38UCSC Ensembl
Innerchr19:12516150..12544872hg19UCSC Ensembl
Innerchr19:12377150..12405872hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3828723
hg1928723
hg1828723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3434n100
Supporting Variantsnssv3564725, nssv3564724
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)nsv1059474
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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