A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564675



Internal ID18862956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8684212..8768019hg38UCSC Ensembl
Innerchr19:8794475..8878695hg19UCSC Ensembl
Innerchr19:8655475..8739695hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3883808
hg1984221
hg1884221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061653
Supporting Variants
Samples
Known GenesACTL9, OR2Z1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564675
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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