A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187127



Internal ID20754167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66046985..66312311hg38UCSC Ensembl
chr15:66339323..66604649hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38265327
hg19265327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509946
Supporting Variants
Samples
Known GenesDIS3L, MEGF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187127
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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