A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495361



Internal ID272478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95568462..95570924hg38UCSC Ensembl
chr12:95962238..95964700hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382463
hg192463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17684252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495361
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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