A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716204



Internal ID139870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10325345..10345662hg38UCSC Ensembl
chr18:10325342..10345659hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3820318
hg1920318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531736
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716204
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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