A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16916155



Internal ID11489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75136244..75149578hg38UCSC Ensembl
chr2:75363370..75376704hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3813335
hg1913335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436009
Supporting Variants
Samples
Known GenesTACR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16916155
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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