A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482909



Internal ID21140462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68922449..69176647hg38UCSC Ensembl
chr13:69496581..69750779hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38254199
hg19254199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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