A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504273



Internal ID281080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98563024..98569232hg38UCSC Ensembl
chr12:98956802..98963010hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg386209
hg196209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17690208
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504273
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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