A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688002



Internal ID111668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56043448..56115004hg38UCSC Ensembl
chr13:56617582..56689138hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3871557
hg1971557
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688002
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.141118


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