A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17055577



Internal ID104883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32394214..32397216hg38UCSC Ensembl
chr12:32547148..32550150hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg383003
hg193003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513755
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17055577
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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