A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007548



Internal ID21916891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43580895..43580947hg38UCSC Ensembl
chr6:43548632..43548684hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565078
Samples
Known GenesPOLH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007548
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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