A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067364



Internal ID19156583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36430302..36494972hg38UCSC Ensembl
Innerchr19:36921204..36985874hg19UCSC Ensembl
Innerchr19:41613044..41677714hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3864671
hg1964671
hg1864671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568186
Samples
Known GenesLOC728752, ZNF566
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067364
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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