A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494609



Internal ID21152162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40531563..40537488hg38UCSC Ensembl
chr13:41105700..41111625hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg385926
hg195926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008905
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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