A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032591



Internal ID21941934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58484217..58485484hg38UCSC Ensembl
chr15:58776416..58777683hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381268
hg191268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599641
Samples
Known GenesLIPC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032591
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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