A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578516



Internal ID16019239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7691102..7693453hg38UCSC Ensembl
Innerchr19:7755988..7758339hg19UCSC Ensembl
Innerchr19:7661988..7664339hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382352
hg192352
hg182352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6248n54
Supporting Variantsnssv893257, nssv893258, nssv893259, nssv893260, nssv893261, nssv893256
Samples
Known GenesFCER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578516
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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