A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578522



Internal ID16019245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7691153..7694144hg38UCSC Ensembl
Innerchr19:7756039..7759030hg19UCSC Ensembl
Innerchr19:7662039..7665030hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382992
hg192992
hg182992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893272
Samples
Known GenesFCER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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