A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6579n54



Internal ID20140003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54778505..54821146hg38UCSC Ensembl
chr19:55289957..55332601hg19UCSC Ensembl
chr19:59981769..60024413hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3842642
hg1942645
hg1842645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580321, nsv580324, nsv580323, nsv580322, nsv580325
Samples
Known GenesKIR2DL1, KIR2DL4, KIR3DL1, LOC100287534
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6579n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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