A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943068



Internal ID22718512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:55057329..55057788hg38UCSC Ensembl
chr13:55631464..55631923hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943068
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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