A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904782



Internal ID22679960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165974126..165974436hg38UCSC Ensembl
chr4:166895278..166895588hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415030
Samples
Known GenesTLL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904782
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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