A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001958



Internal ID21911301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100727331..100727398hg38UCSC Ensembl
chr8:101739559..101739626hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001958
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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