A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6195n54



Internal ID18998371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1137713..1152657hg38UCSC Ensembl
chr19:1137712..1152656hg19UCSC Ensembl
chr19:1088712..1103656hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3814945
hg1914945
hg1814945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578263, nsv578266, nsv578264, nsv578262, nsv578259, nsv578261, nsv578256
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6195n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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