A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265978



Internal ID20475196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69601740..69607085hg38UCSC Ensembl
chr4:70467458..70472803hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg385346
hg195346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731132
Supporting Variants
Samples
Known GenesUGT2A1, UGT2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265978
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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