A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515682



Internal ID15443293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96585044..96598920hg38UCSC Ensembl
Innerchr3:96303888..96317764hg19UCSC Ensembl
Innerchr3:97786578..97800454hg18UCSC Ensembl
Innerchr3:97786578..97800454hg17UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3813877
hg1913877
hg1813877
hg1713877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664371, nssv662702, nssv660477, nssv673515, nssv677481, nssv671419, nssv686364, nssv693317
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515682
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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