A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694434



Internal ID118100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93987281..93988957hg38UCSC Ensembl
chr13:94639535..94641211hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554850
Supporting Variants
Samples
Known GenesGPC6
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694434
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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