A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516391



Internal ID15443684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:190385199..190390667hg38UCSC Ensembl
Innerchr3:190102988..190108456hg19UCSC Ensembl
Innerchr3:191585682..191591150hg18UCSC Ensembl
Innerchr3:191585690..191591158hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg385469
hg195469
hg185469
hg175469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688072, nssv684509, nssv699359, nssv667996
Samples
Known GenesCLDN16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516391
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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