A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716657



Internal ID140323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23604085..23604595hg38UCSC Ensembl
chr18:21184049..21184559hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530619
Supporting Variants
Samples
Known GenesANKRD29
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716657
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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