A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369882



Internal ID22595551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35864267..35864584hg38UCSC Ensembl
chr13:36438404..36438721hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934917
Supporting Variants
Samples
Known GenesDCLK1, MIR548F5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369882
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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