A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526289



Internal ID15453582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16918311..16934051hg38UCSC Ensembl
Innerchr17:16821625..16837365hg19UCSC Ensembl
Innerchr17:16762350..16778090hg18UCSC Ensembl
Innerchr17:16762350..16778090hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3815741
hg1915741
hg1815741
hg1715741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702570
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526289
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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