A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525724



Internal ID301873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12755783..12756318hg38UCSC Ensembl
chr18:12755782..12756317hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525724
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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