A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515876



Internal ID6014522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43116906..43445305hg19UCSC Ensembl
Innerchr15:40904198..41232597hg18UCSC Ensembl
Innerchr15:40904198..41232597hg17UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain+Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv705714, nssv695338, nssv705373, nssv669551, nssv665118, nssv682487, nssv662075, nssv705701
Samples
Known GenesTMEM62, TTBK2, UBR1
Method
AnalysisMerged-level CNV regions
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv515876
Frequency
Sample Size2026
Observed Gain6
Observed Loss2
Observed Complex0
Frequencyn/a


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