A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3677n100



Internal ID20155293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54819187..54868123hg38UCSC Ensembl
chr19:55330642..55379578hg19UCSC Ensembl
chr19:60022454..60071390hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3848937
hg1948937
hg1848937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060564, nsv1065329
Samples
Known GenesKIR2DS4, KIR3DL1, KIR3DL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3677n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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