A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525796



Internal ID15106403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40150112..40248785hg38UCSC Ensembl
Innerchr17:38306365..38405037hg19UCSC Ensembl
Innerchr17:35559891..35658563hg18UCSC Ensembl
Innerchr17:35559891..35658563hg17UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg3898674
hg1998673
hg1898673
hg1798673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701978
Samples
Known GenesCASC3, MIR6866, MIR6867, RAPGEFL1, WIPF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525796
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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