A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6248n54



Internal ID22774143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7690993..7693584hg38UCSC Ensembl
chr19:7755879..7758470hg19UCSC Ensembl
chr19:7661879..7664470hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382592
hg192592
hg182592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578526, nsv578527, nsv578515, nsv578528, nsv578520, nsv578523, nsv578525, nsv578512, nsv578529, nsv578513, nsv578516, nsv578517, nsv578521
Samples
Known GenesFCER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6248n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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