A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578527



Internal ID16019250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7691330..7693584hg38UCSC Ensembl
Innerchr19:7756216..7758470hg19UCSC Ensembl
Innerchr19:7662216..7664470hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382255
hg192255
hg182255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6248n54
Supporting Variantsnssv893288, nssv893287, nssv893289
Samples
Known GenesFCER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578527
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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