A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522888



Internal ID299144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26750306..26760967hg38UCSC Ensembl
chr18:24330270..24340931hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3810662
hg1910662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522888
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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