A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716399



Internal ID140065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13918346..13919778hg38UCSC Ensembl
chr18:13918345..13919777hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381433
hg191433
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716399
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.03325


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