A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522839



Internal ID299097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71497600..71782669hg38UCSC Ensembl
chr18:69164836..69449905hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38285070
hg19285070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719296
Samples
Known GenesLOC100505776
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522839
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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