A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140892



Internal ID340086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158998122..158999299hg38UCSC Ensembl
chr6:159419154..159420331hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381178
hg191178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989552
Samples
Known GenesRSPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140892
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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