A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926998



Internal ID18713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234559311..234607443hg38UCSC Ensembl
chr2:235467955..235516087hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3848133
hg1948133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445481
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926998
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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