A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282573



Internal ID20491791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50307880..50308007hg38UCSC Ensembl
chr3:50345311..50345438hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742682
Supporting Variants
Samples
Known GenesHYAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282573
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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