A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518578



Internal ID15099185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48475068..48510834hg38UCSC Ensembl
Innerchr19:48978325..49014091hg19UCSC Ensembl
Innerchr19:53670137..53705903hg18UCSC Ensembl
Innerchr19:53670137..53705903hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3835767
hg1935767
hg1835767
hg1735767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696022
Samples
Known GenesCYTH2, LMTK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518578
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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