A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155833



Internal ID22086338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:58257886..58267654hg38UCSC Ensembl
Outerchr1:58254237..58276798hg38UCSC Ensembl
Innerchr1:58723558..58733326hg19UCSC Ensembl
Outerchr1:58719909..58742470hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3822562
hg1922562
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015242
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155833
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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