A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578514



Internal ID16365923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7691102..7692580hg38UCSC Ensembl
Innerchr19:7755988..7757466hg19UCSC Ensembl
Innerchr19:7661988..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 Variantsdgv6249n54
Supporting Variantsnssv893252, nssv893251
Samples
Known GenesFCER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578514
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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