A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155174



Internal ID22085679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46838203..46924708hg38UCSC Ensembl
Outerchr15:46836155..46929167hg38UCSC Ensembl
Innerchr15:47130401..47216906hg19UCSC Ensembl
Outerchr15:47128353..47221365hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3893013
hg1993013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011068
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155174
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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