A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564695



Internal ID18516290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11236671..11271344hg38UCSC Ensembl
Innerchr19:11347347..11382020hg19UCSC Ensembl
Innerchr19:11208347..11243020hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3834674
hg1934674
hg1834674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060605
Supporting Variants
Samples
Known GenesC19orf80, DOCK6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564695
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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