A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522060



Internal ID15449353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13896600..13904892hg38UCSC Ensembl
Innerchr17:13799917..13808209hg19UCSC Ensembl
Innerchr17:13740642..13748934hg18UCSC Ensembl
Innerchr17:13740642..13748934hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg388293
hg198293
hg188293
hg178293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694831
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522060
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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