A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16911033



Internal ID8125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26529930..26529947hg38UCSC Ensembl
chr2:26752798..26752815hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541982
Supporting Variants
Samples
Known GenesOTOF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16911033
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.206207


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