A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957829



Internal ID39198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165957586..165979993hg38UCSC Ensembl
chr4:166878738..166901145hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3822408
hg1922408
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466252
Supporting Variants
Samples
Known GenesTLL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957829
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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