A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564767



Internal ID18516362
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 StatusS
Merged Variantsnsv1062216
Supporting Variants
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)nssv3564767
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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