A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524553



Internal ID15105160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15744409..15776287hg38UCSC Ensembl
Innerchr17:15647723..15679601hg19UCSC Ensembl
Innerchr17:15588448..15620326hg18UCSC Ensembl
Innerchr17:15588448..15620326hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3831879
hg1931879
hg1831879
hg1731879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700505
Samples
Known GenesCDRT15P2, TBC1D26
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524553
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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