A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371155



Internal ID22596824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56271587..56272638hg38UCSC Ensembl
chr13:56845721..56846772hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg381052
hg191052
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943281
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371155
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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