A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500860



Internal ID20874089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81113301..81120100hg38UCSC Ensembl
chr15:81405642..81412441hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2606n223
Supporting Variantsnssv18178886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500860
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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