A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062216



Internal ID18804747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12454604..12568009hg38UCSC Ensembl
Innerchr19:12565418..12678823hg19UCSC Ensembl
Innerchr19:12426418..12539823hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38113406
hg19113406
hg18113406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3436n100
Supporting Variantsnssv3564767
Samples
Known GenesZNF564, ZNF709
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062216
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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