A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518765



Internal ID15446058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15724015..15741192hg38UCSC Ensembl
Innerchr17:15627329..15644506hg19UCSC Ensembl
Innerchr17:15568054..15585231hg18UCSC Ensembl
Innerchr17:15568054..15585231hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3817178
hg1917178
hg1817178
hg1717178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694272
Samples
Known GenesTBC1D26
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518765
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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