A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015162



Internal ID21924505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66830148..66833275hg38UCSC Ensembl
chr8:67742383..67745510hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg383128
hg193128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583389
Samples
Known GenesC8orf44-SGK3, SGK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015162
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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