A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17349947



Internal ID22575616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102829401..102831498hg38UCSC Ensembl
chr13:103481751..103483848hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382098
hg192098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934556
Supporting Variants
Samples
Known GenesBIVM, BIVM-ERCC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17349947
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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