A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019724



Internal ID21929067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123646840..123652500hg38UCSC Ensembl
chr8:124659080..124664740hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg385661
hg195661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582905
Samples
Known GenesKLHL38
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019724
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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