A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526532



Internal ID15107139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93027493..93053776hg38UCSC Ensembl
Innerchr15:93570723..93597006hg19UCSC Ensembl
Innerchr15:91371727..91398010hg18UCSC Ensembl
Innerchr15:91371727..91398010hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3826284
hg1926284
hg1826284
hg1726284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv157n21
Supporting Variantsnssv702845
Samples
Known GenesCHD2, RGMA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526532
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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