A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3492n100



Internal ID22789579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:24320958..24413936hg38UCSC Ensembl
chr19:24503760..24596738hg19UCSC Ensembl
chr19:24295600..24388578hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg3892979
hg1992979
hg1892979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060092, nsv1065214, nsv1061623, nsv1056577
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3492n100
Frequency
Sample Size11257
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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