A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008939



Internal ID21918282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:99888300..99889824hg38UCSC Ensembl
chr8:100900528..100902052hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg381525
hg191525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578414
Samples
Known GenesCOX6C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008939
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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