A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020237



Internal ID21929580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113906321..113906376hg38UCSC Ensembl
chr6:114227485..114227540hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564897
Samples
Known GenesFLJ34503
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020237
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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