A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579358



Internal ID16366767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35169767..35172830hg38UCSC Ensembl
Innerchr19:35660670..35663733hg19UCSC Ensembl
Innerchr19:40352510..40355573hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383064
hg193064
hg183064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898597
Samples
Known GenesFXYD5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579358
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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