A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17054914



Internal ID104444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2895748..2898065hg38UCSC Ensembl
chr12:3004914..3007231hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg382318
hg192318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497274
Supporting Variants
Samples
Known GenesTULP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17054914
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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