A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515890



Internal ID15442947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17794865..17799635hg38UCSC Ensembl
Innerchr11:17816412..17821182hg19UCSC Ensembl
Innerchr11:17772988..17777758hg18UCSC Ensembl
Innerchr11:17772988..17777758hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384771
hg194771
hg184771
hg174771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665165, nssv669740
Samples
Known GenesSERGEF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515890
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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