A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3669n100



Internal ID20155285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54736428..54822417hg38UCSC Ensembl
chr19:55247895..55333872hg19UCSC Ensembl
chr19:59939707..60025684hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3885990
hg1985978
hg1885978
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059091, nsv1061438, nsv1061067, nsv1055171, nsv1064985, nsv1064780, nsv1064703
Samples
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR3DL1, KIR3DL3, LOC100287534
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3669n100
Frequency
Sample Size29084
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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