A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6249n54



Internal ID22774144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7691102..7692580hg38UCSC Ensembl
chr19:7755988..7757466hg19UCSC Ensembl
chr19:7661988..7663466hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381479
hg191479
hg181479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578514, nsv578524, nsv578519
Samples
Known GenesFCER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6249n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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