A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058164



Internal ID18800695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358159..35387466hg38UCSC Ensembl
Innerchr19:35849061..35878368hg19UCSC Ensembl
Innerchr19:40540901..40570208hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3829308
hg1929308
hg1829308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3520n100
Supporting Variantsnssv3566628
Samples
Known GenesFFAR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058164
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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