A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518908



Internal ID15446201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117180449..117195974hg38UCSC Ensembl
Innerchr11:117051165..117066690hg19UCSC Ensembl
Innerchr11:116556375..116571900hg18UCSC Ensembl
Innerchr11:116556375..116571900hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3815526
hg1915526
hg1815526
hg1715526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696368
Samples
Known GenesLOC100652768, SIDT2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518908
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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