A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3670n100



Internal ID20155286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54736428..54836508hg38UCSC Ensembl
chr19:55247895..55347963hg19UCSC Ensembl
chr19:59939707..60039775hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38100081
hg19100069
hg18100069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064632, nsv1064167, nsv1063499, nsv1056504, nsv1063202
Samples
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR2DS4, 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)dgv3670n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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