A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717047



Internal ID140713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30938072..30950110hg38UCSC Ensembl
chr18:28518038..28530076hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3812039
hg1912039
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563438
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717047
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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