A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032637



Internal ID21941980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64479355..64479456hg38UCSC Ensembl
chr17:62475472..62475573hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628712
Samples
Known GenesPOLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032637
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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