A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478933



Internal ID256476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:530050..594342hg38UCSC Ensembl
chr10:575990..640282hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3864293
hg1964293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030829
Samples
Known GenesDIP2C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478933
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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