A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523923



Internal ID15451216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:11312688..11318762hg38UCSC Ensembl
Innerchr17:11216005..11222079hg19UCSC Ensembl
Innerchr17:11156730..11162804hg18UCSC Ensembl
Innerchr17:11156730..11162804hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg386075
hg196075
hg186075
hg176075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699768
Samples
Known GenesSHISA6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523923
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