A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154062



Internal ID19196556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:68406458..68411959hg38UCSC Ensembl
Outerchr17:66402599..66408100hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg385502
hg195502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003337
SamplesKWB1
Known GenesARSG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1154062
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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