A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493862



Internal ID271027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19517993..19750318hg38UCSC Ensembl
chr10:19806922..20039247hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38232326
hg19232326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv43n206
Supporting Variantsnssv17033599
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493862
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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