A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578528



Internal ID16019251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7691453..7693374hg38UCSC Ensembl
Innerchr19:7756339..7758260hg19UCSC Ensembl
Innerchr19:7662339..7664260hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381922
hg191922
hg181922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6248n54
Supporting Variantsnssv893291, nssv893290
Samples
Known GenesFCER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578528
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer