A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001852



Internal ID21911195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96376368..96376565hg38UCSC Ensembl
chr8:97388596..97388793hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001852
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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