A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521515



Internal ID15102122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6855195..6957288hg38UCSC Ensembl
Innerchr17:6758514..6860607hg19UCSC Ensembl
Innerchr17:6699238..6801331hg18UCSC Ensembl
Innerchr17:6699238..6801331hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38102094
hg19102094
hg18102094
hg17102094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698132
Samples
Known GenesALOX12P2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521515
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