A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716330



Internal ID139996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12777034..12777616hg38UCSC Ensembl
chr18:12777033..12777615hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523660
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716330
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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