A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519824



Internal ID15447117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68463499..68464362hg38UCSC Ensembl
Innerchr15:68755838..68756701hg19UCSC Ensembl
Innerchr15:66542892..66543755hg18UCSC Ensembl
Innerchr15:66542892..66543755hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38864
hg19864
hg18864
hg17864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677611, nssv671998, nssv658947
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519824
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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