A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520301



Internal ID15447594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27332262..27333163hg38UCSC Ensembl
Innerchr17:25659288..25660189hg19UCSC Ensembl
Innerchr17:22683415..22684316hg18UCSC Ensembl
Innerchr17:22683415..22684316hg17UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg38902
hg19902
hg18902
hg17902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682149, nssv662654
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520301
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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