A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716558



Internal ID140224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21759422..21759473hg38UCSC Ensembl
chr18:19339383..19339434hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553106
Supporting Variants
Samples
Known GenesMIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716558
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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