A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192816



Internal ID20759856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99281636..99584493hg38UCSC Ensembl
chr15:99821841..100124698hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38302858
hg19302858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514283
Supporting Variants
Samples
Known GenesLRRC28, MEF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192816
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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