A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515875



Internal ID15442932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24821213..24843068hg38UCSC Ensembl
Innerchr15:25066360..25088215hg19UCSC Ensembl
Innerchr15:22617453..22639308hg18UCSC Ensembl
Innerchr15:22617453..22639308hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3821856
hg1921856
hg1821856
hg1721856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667266, nssv661789, nssv681157, nssv685959, nssv692118, nssv678048, nssv690037, nssv665117, nssv704101, nssv671395
Samples
Known GenesSNRPN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515875
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