A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687039



Internal ID110705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39454344..39454654hg38UCSC Ensembl
chr13:40028481..40028791hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507460
Supporting Variants
Samples
Known GenesLHFP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687039
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.641586


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