A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900920



Internal ID1413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2837152..2837737hg38UCSC Ensembl
chr2:2840924..2841509hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900920
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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