A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564757



Internal ID18863038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12408389..12447619hg38UCSC Ensembl
Innerchr19:12519203..12558433hg19UCSC Ensembl
Innerchr19:12380203..12419433hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3839231
hg1939231
hg1839231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063309
Supporting Variants
Samples
Known GenesZNF443
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564757
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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