A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518083



Internal ID15445376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97463272..97493001hg38UCSC Ensembl
Innerchr15:98006502..98036231hg19UCSC Ensembl
Innerchr15:95807506..95837235hg18UCSC Ensembl
Innerchr15:95807506..95837235hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3829730
hg1929730
hg1829730
hg1729730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695496
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518083
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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