A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522419



Internal ID15103026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99786862..100083500hg38UCSC Ensembl
Innerchr15:100327067..100623705hg19UCSC Ensembl
Innerchr15:98144590..98441228hg18UCSC Ensembl
Innerchr15:98144590..98441228hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38296639
hg19296639
hg18296639
hg17296639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705772
Samples
Known GenesADAMTS17, DNM1P46
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522419
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