A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010840



Internal ID21920183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93936739..93936870hg38UCSC Ensembl
chr8:94948967..94949098hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010840
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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