A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578534



Internal ID16019257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7692252..7694790hg38UCSC Ensembl
Innerchr19:7757138..7759676hg19UCSC Ensembl
Innerchr19:7663138..7665676hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382539
hg192539
hg182539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6251n54
Supporting Variantsnssv893299
Samples
Known GenesFCER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578534
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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