A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507919



Internal ID284624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32465465..32473883hg38UCSC Ensembl
chr12:32618399..32626817hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg388419
hg198419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17055587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507919
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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