A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716239



Internal ID139905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11825496..11829883hg38UCSC Ensembl
chr18:11825495..11829882hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg384388
hg194388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524956
Supporting Variants
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716239
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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