A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579523



Internal ID16366932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39896716..39902512hg38UCSC Ensembl
Innerchr19:40387356..40392585hg19UCSC Ensembl
Innerchr19:45079196..45084425hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385797
hg195230
hg185230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899385
Samples
Known GenesFCGBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579523
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