A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015168



Internal ID21924511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93936160..93949790hg38UCSC Ensembl
chr8:94948388..94962018hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3813631
hg1913631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015168
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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