A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568184



Internal ID18866465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36410108..36465349hg38UCSC Ensembl
Innerchr19:36901010..36956251hg19UCSC Ensembl
Innerchr19:41592850..41648091hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3855242
hg1955242
hg1855242
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067101
Supporting Variants
Samples
Known GenesLOC644189, ZFP82, ZNF566
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568184
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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