A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3668n100



Internal ID20155284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54725768..54868189hg38UCSC Ensembl
chr19:55237234..55379644hg19UCSC Ensembl
chr19:59929046..60071456hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38142422
hg19142411
hg18142411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060821, nsv1060311, nsv1058209, nsv1062404, nsv1057898, nsv1065979, nsv1056383, nsv1060064, nsv1060745, nsv1067447
Samples
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, 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)dgv3668n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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