A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6551n54



Internal ID22774446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54223279..54240481hg38UCSC Ensembl
chr19:54727151..54744358hg19UCSC Ensembl
chr19:59418963..59436170hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3817203
hg1917208
hg1817208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580183, nsv580169, nsv580184, nsv580160, nsv580163, nsv580171, nsv580162, nsv580185, nsv580189, nsv580172, nsv580190, nsv580170
Samples1780862584_A, HGDP00472, HGDP01419
Known GenesLILRA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6551n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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