A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005374



Internal ID21914717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54060825..54061986hg38UCSC Ensembl
chr8:54973385..54974546hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg381162
hg191162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593487
Samples
Known GenesLYPLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005374
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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