A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526307



Internal ID15106914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:49329551..49363058hg38UCSC Ensembl
Innerchr17:47406913..47440420hg19UCSC Ensembl
Innerchr17:44761912..44795419hg18UCSC Ensembl
Innerchr17:44761912..44795419hg17UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3833508
hg1933508
hg1833508
hg1733508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702590
Samples
Known GenesZNF652
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526307
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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