A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6578n54



Internal ID20140002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54772850..54786119hg38UCSC Ensembl
chr19:55284302..55297571hg19UCSC Ensembl
chr19:59976114..59989383hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3813270
hg1913270
hg1813270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580319, nsv580317
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6578n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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