A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706491



Internal ID21378767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9516687..9518765hg38UCSC Ensembl
chr20:9497334..9499412hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg382079
hg192079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392460
Supporting Variants
Samples
Known GenesLAMP5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706491
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0143678


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