A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450772



Internal ID22508645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68848301..68851675hg38UCSC Ensembl
chr13:69422433..69425807hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg383375
hg193375
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854627
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450772
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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