A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010754



Internal ID21920097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38522787..38522893hg38UCSC Ensembl
chr8:38380305..38380411hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558943
Samples
Known GenesC8orf86
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010754
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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