A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693322



Internal ID116988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79599488..79599646hg38UCSC Ensembl
chr13:80173623..80173781hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556954
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693322
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000624


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