A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519210



Internal ID15446503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8980461..8986824hg38UCSC Ensembl
Innerchr17:8883778..8890141hg19UCSC Ensembl
Innerchr17:8824503..8830866hg18UCSC Ensembl
Innerchr17:8824503..8830866hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg386364
hg196364
hg186364
hg176364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696700
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519210
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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