A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17011665



Internal ID75438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54076147..54076275hg38UCSC Ensembl
chr8:54988707..54988835hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478700
Supporting Variants
Samples
Known GenesLYPLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17011665
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003278


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