A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17718256



Internal ID141922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53254662..53254676hg38UCSC Ensembl
chr18:50781032..50781046hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3815
hg1915
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560431
Supporting Variants
Samples
Known GenesDCC
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17718256
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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