A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149415



Internal ID19195093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:44286341..44286675hg38UCSC Ensembl
Outerchr15:44578539..44578873hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000720
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149415
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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