A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526222



Internal ID15453515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69565323..69566223hg38UCSC Ensembl
Innerchr15:69857662..69858562hg19UCSC Ensembl
Innerchr15:67644716..67645616hg18UCSC Ensembl
Innerchr15:67644716..67645616hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38901
hg19901
hg18901
hg17901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702487
Samples
Known GenesLOC145837
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526222
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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