A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482393



Internal ID259850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30510775..30514172hg38UCSC Ensembl
chr10:30799704..30803101hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg383398
hg193398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482393
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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