A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389226



Internal ID22447096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82413589..82416151hg38UCSC Ensembl
chr13:82987724..82990286hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg382563
hg192563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389226
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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