A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067486



Internal ID19156705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12405336..12431081hg38UCSC Ensembl
Innerchr19:12516150..12541895hg19UCSC Ensembl
Innerchr19:12377150..12402895hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3825746
hg1925746
hg1825746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3433n100
Supporting Variantsnssv3564722, nssv3564720, nssv3564719, nssv3564715, nssv3564723, nssv3564718, nssv3564721, nssv3564717, nssv3723289, nssv3564716
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)nsv1067486
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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