A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564768



Internal ID18516363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12454604..12581187hg38UCSC Ensembl
Innerchr19:12565418..12692001hg19UCSC Ensembl
Innerchr19:12426418..12553001hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38126584
hg19126584
hg18126584
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060358
Supporting Variants
Samples
Known GenesZNF490, ZNF564, ZNF709
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564768
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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