A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563360



Internal ID21887715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158892891..158897617hg38UCSC Ensembl
chr6:159313923..159318649hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384727
hg194727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006806
Supporting Variants
Samples
Known GenesC6orf99
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563360
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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