A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6497n54



Internal ID22774392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43158934..43349353hg38UCSC Ensembl
chr19:43663086..43853505hg19UCSC Ensembl
chr19:48354926..48545345hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38190420
hg19190420
hg18190420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579825, nsv579819, nsv579818, nsv579816, nsv579817
SamplesHGDP00057
Known GenesLOC284344, PRG1, PSG4, PSG5, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6497n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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