A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517448



Internal ID15098055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4875696..4878596hg38UCSC Ensembl
Innerchr19:4875708..4878608hg19UCSC Ensembl
Innerchr19:4826708..4829608hg18UCSC Ensembl
Innerchr19:4826708..4829608hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382901
hg192901
hg182901
hg172901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678143, nssv688575, nssv667709, nssv687867, nssv663984, nssv677896, nssv667525, nssv652047, nssv701000, nssv652800
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517448
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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