A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052906



Internal ID103122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10341287..10341519hg38UCSC Ensembl
chr12:10493886..10494118hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052906
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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