A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018226



Internal ID21927569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96057623..96057679hg38UCSC Ensembl
chr8:97069851..97069907hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018226
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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