A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479126



Internal ID21136679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75593801..75598580hg38UCSC Ensembl
chr13:76167937..76172716hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg384780
hg194780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013368
Samples
Known GenesUCHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479126
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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