A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521892



Internal ID15449185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69898813..69961547hg38UCSC Ensembl
Innerchr17:67894954..67957688hg19UCSC Ensembl
Innerchr17:65406549..65469283hg18UCSC Ensembl
Innerchr17:65406549..65469283hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3862735
hg1962735
hg1862735
hg1762735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694664
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521892
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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