A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061792



Internal ID18804323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54073048..54101539hg38UCSC Ensembl
Innerchr19:54576302..54604822hg19UCSC Ensembl
Innerchr19:59268114..59296634hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3828492
hg1928521
hg1828521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3653n100
Supporting Variantsnssv3726550
Samples
Known GenesOSCAR, TARM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061792
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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