A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147123



Internal ID18851845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:84220347..84225648hg38UCSC Ensembl
Outerchr15:84889099..84894400hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg385302
hg195302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998485
SamplesKWB1
Known GenesLOC388152
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147123
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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