A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529685



Internal ID305695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10402986..10405470hg38UCSC Ensembl
chr18:10402983..10405467hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg382485
hg192485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529685
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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