A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942676



Internal ID22718118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58704724..58705024hg38UCSC Ensembl
chr18:56371956..56372256hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370496
Samples
Known GenesMALT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942676
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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