A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687020



Internal ID110686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38953803..38955890hg38UCSC Ensembl
chr13:39527940..39530027hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg382088
hg192088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687020
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006556


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