A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268539



Internal ID20477757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54059296..54059610hg38UCSC Ensembl
chr8:54971856..54972170hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743877
Supporting Variants
Samples
Known GenesLYPLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268539
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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