A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937600



Internal ID25782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126158824..126158878hg38UCSC Ensembl
chr3:125877667..125877721hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439714
Supporting Variants
Samples
Known GenesALDH1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937600
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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