A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927987



Internal ID19366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:205921423..205921474hg38UCSC Ensembl
chr2:206786147..206786198hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381204
hg191204
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927987
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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