A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532321



Internal ID308247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9434957..9436202hg38UCSC Ensembl
chr18:9434955..9436200hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532321
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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