A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910675



Internal ID7888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28250008..28253827hg38UCSC Ensembl
chr2:28472875..28476694hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg383820
hg193820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452269
Supporting Variants
Samples
Known GenesBRE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910675
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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