A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478099



Internal ID21135652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85940091..85992561hg38UCSC Ensembl
chr13:86514226..86566696hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3852471
hg1952471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014781
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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