A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6502n54



Internal ID20139926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43290434..43366735hg38UCSC Ensembl
chr19:43794586..43870887hg19UCSC Ensembl
chr19:48486426..48562727hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3876302
hg1976302
hg1876302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579843, nsv579842
Samples
Known GenesCD177, PRG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6502n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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