A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148906



Internal ID18851133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41624440..41624497hg38UCSC Ensembl
Outerchr15:41916638..41916695hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997692
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148906
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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