A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526441



Internal ID15107048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3604947..3735456hg38UCSC Ensembl
Innerchr11:3626177..3756686hg19UCSC Ensembl
Innerchr11:3582753..3713262hg18UCSC Ensembl
Innerchr11:3582753..3713262hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38130510
hg19130510
hg18130510
hg17130510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702744
Samples
Known GenesART1, ART5, CHRNA10, NUP98, TRPC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526441
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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