A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018067



Internal ID21927410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1840400..1840495hg38UCSC Ensembl
chr8:1788566..1788661hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576987
Samples
Known GenesARHGEF10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018067
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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