A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155151



Internal ID22085656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32478259hg38UCSC Ensembl
Outerchr15:32151995..32484010hg38UCSC Ensembl
Innerchr15:32458661..32770460hg19UCSC Ensembl
Outerchr15:32444196..32776211hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38332016
hg19332016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011018
Samples
Known GenesCHRNA7, GOLGA8K, GOLGA8O, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155151
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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