A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518888



Internal ID15446181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19886140..19900934hg38UCSC Ensembl
Innerchr17:19789453..19804247hg19UCSC Ensembl
Innerchr17:19730045..19744839hg18UCSC Ensembl
Innerchr17:19730045..19744839hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3814795
hg1914795
hg1814795
hg1714795
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694285
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518888
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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