A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957832



Internal ID39200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165974136..165974437hg38UCSC Ensembl
chr4:166895288..166895589hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463465
Supporting Variants
Samples
Known GenesTLL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957832
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.086794


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