A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528369



Internal ID15108976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40100440..40132750hg38UCSC Ensembl
Innerchr17:38256693..38289003hg19UCSC Ensembl
Innerchr17:35510219..35542529hg18UCSC Ensembl
Innerchr17:35510219..35542529hg17UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg3832311
hg1932311
hg1832311
hg1732311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704956
Samples
Known GenesMSL1, NR1D1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528369
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