A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456998



Internal ID22514879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50104012..50105258hg38UCSC Ensembl
chr13:50678148..50679394hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381247
hg191247
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861317
Supporting Variants
Samples
Known GenesDLEU1, DLEU2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456998
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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