A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481685



Internal ID259154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24826826..24832055hg38UCSC Ensembl
chr10:25115755..25120984hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385230
hg195230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481685
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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