A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686868



Internal ID110534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35850678..35850802hg38UCSC Ensembl
chr13:36424815..36424939hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495134
Supporting Variants
Samples
Known GenesDCLK1, MIR548F5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686868
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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