A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564711



Internal ID18862992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12395059..12435375hg38UCSC Ensembl
Innerchr19:12505873..12546189hg19UCSC Ensembl
Innerchr19:12366873..12407189hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3840317
hg1940317
hg1840317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055540
Supporting Variants
Samples
Known GenesZNF443, ZNF799
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564711
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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