A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515800



Internal ID15442857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:17418882..17441339hg38UCSC Ensembl
Innerchr17:17322196..17344653hg19UCSC Ensembl
Innerchr17:17262921..17285378hg18UCSC Ensembl
Innerchr17:17262921..17285378hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3822458
hg1922458
hg1822458
hg1722458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664821, nssv668349
Samples
Known GenesSMCR9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515800
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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