A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516596



Internal ID15443889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24847119..24869979hg38UCSC Ensembl
Innerchr15:25092266..25115126hg19UCSC Ensembl
Innerchr15:22643359..22666219hg18UCSC Ensembl
Innerchr15:22643359..22666219hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3822861
hg1922861
hg1822861
hg1722861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663069, nssv678187, nssv671705, nssv652459, nssv693932, nssv664975, nssv670236, nssv662195, nssv660369, nssv686101, nssv651938, nssv655083, nssv662164, nssv666551, nssv688926, nssv669050, nssv652596, nssv694196, nssv668543, nssv673177, nssv681827, nssv690342, nssv666782, nssv652886, nssv692488, nssv679195, nssv656969, nssv689750, nssv684906, nssv672071, nssv691105, nssv657275, nssv673475, nssv670161, nssv692535, nssv692169, nssv657533
Samples
Known GenesSNRPN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516596
Frequency
Sample Size2026
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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