A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922868



Internal ID16003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200935284..200935410hg38UCSC Ensembl
chr2:201800007..201800133hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439097
Supporting Variants
Samples
Known GenesORC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922868
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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