A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493957



Internal ID21151510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68406725..68655706hg38UCSC Ensembl
chr13:68980857..69229838hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38248982
hg19248982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194982
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493957
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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