A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514283



Internal ID20887635
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 StatusM
Merged Variants
Supporting Variantsnssv18192816
Samples
Known GenesLRRC28, MEF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514283
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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