A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17719684



Internal ID143350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77130979..77130979hg38UCSC Ensembl
chr18:74842935..74842935hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561906
Supporting Variants
Samples
Known GenesMBP
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17719684
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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