A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529992



Internal ID305990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74806505..74829312hg38UCSC Ensembl
chr18:72518461..72541268hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3822808
hg1922808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719506
Samples
Known GenesZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529992
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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