A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684223



Internal ID107889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95037754..95037772hg38UCSC Ensembl
chr12:95431530..95431548hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534480
Supporting Variants
Samples
Known GenesNR2C1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684223
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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