A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564712



Internal ID18862993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12395059..12438841hg38UCSC Ensembl
Innerchr19:12505873..12549655hg19UCSC Ensembl
Innerchr19:12366873..12410655hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3843783
hg1943783
hg1843783
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057691
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)nssv3564712
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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