A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516413



Internal ID15097020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18606871..18622211hg38UCSC Ensembl
Innerchr11:18628418..18643758hg19UCSC Ensembl
Innerchr11:18584994..18600334hg18UCSC Ensembl
Innerchr11:18584994..18600334hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3815341
hg1915341
hg1815341
hg1715341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693714, nssv663411, nssv668198
Samples
Known GenesSPTY2D1, SPTY2D1-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516413
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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