A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394727



Internal ID21052280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36000013..36001945hg38UCSC Ensembl
chr5:36000115..36002047hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg381933
hg191933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130429
Samples
Known GenesUGT3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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