A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691514



Internal ID115180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85114235..85115493hg38UCSC Ensembl
chr13:85688370..85689628hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560354
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691514
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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