A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274299



Internal ID20483517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45295003..45300452hg38UCSC Ensembl
chr6:45262740..45268189hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385450
hg195450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741518
Supporting Variants
Samples
Known GenesSUPT3H
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274299
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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