A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944054



Internal ID22719512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73162287..73162812hg38UCSC Ensembl
chr13:73736424..73736949hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944054
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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