A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376109



Internal ID22601778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113954823..113955208hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5946111
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376109
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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