A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16925356



Internal ID17652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142750456..142756523hg38UCSC Ensembl
chr2:143508025..143514092hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg386068
hg196068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16925356
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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