A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526647



Internal ID302771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2858526..2858828hg38UCSC Ensembl
chr18:2858524..2858826hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715887
Samples
Known GenesEMILIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526647
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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