A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510173



Internal ID286800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21010341..21011905hg38UCSC Ensembl
chr12:21163275..21164839hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510173
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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