A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704414



Internal ID21376690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54059290..54059603hg38UCSC Ensembl
chr8:54971850..54972163hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388810
Supporting Variants
Samples
Known GenesLYPLA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704414
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.683908


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