A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015125



Internal ID21924468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13590689..13590758hg38UCSC Ensembl
chr6:13590921..13590990hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575504
Samples
Known GenesSIRT5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015125
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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