A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6192n54



Internal ID18998368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1137402..1138268hg38UCSC Ensembl
chr19:1137401..1138267hg19UCSC Ensembl
chr19:1088401..1089267hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38867
hg19867
hg18867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578242, nsv578249, nsv578243, nsv578253, nsv578247, nsv578250, nsv578252, nsv578236
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6192n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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