A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525382



Internal ID15452675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52500584..52758177hg38UCSC Ensembl
Innerchr17:50577944..50835537hg19UCSC Ensembl
Innerchr17:47932943..48190536hg18UCSC Ensembl
Innerchr17:47932943..48190536hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38257594
hg19257594
hg18257594
hg17257594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701504
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525382
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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