A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16916427



Internal ID11669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104585936..104587726hg38UCSC Ensembl
chr2:105202394..105204184hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg381791
hg191791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447964
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16916427
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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