A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522411



Internal ID6019666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34953986..35462981hg19UCSC Ensembl
Innerchr15:32741278..33250273hg18UCSC Ensembl
Innerchr15:32741278..33250273hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv695193
Samples
Known GenesACTC1, AQR, GJD2, ZNF770
Method
AnalysisCNV regions located outside of or spanning over several merged-level regions determined by the submitter
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv522411
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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