A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152362



Internal ID18848974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:175914796..175943197hg38UCSC Ensembl
Outerchr5:175341799..175370200hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3828402
hg1928402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996969
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152362
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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