A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504823



Internal ID281617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16631998..16632335hg38UCSC Ensembl
chr12:16784932..16785269hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17054389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504823
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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