A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115705



Internal ID19282935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:170240096..170245296hg38UCSC Ensembl
Outerchr5:169667100..169672300hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg385201
hg195201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977513
SamplesKWS2
Known GenesC5orf58
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115705
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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