A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915406



Internal ID11012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100409503..100409655hg38UCSC Ensembl
chr2:101025965..101026117hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437786
Supporting Variants
Samples
Known GenesCHST10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915406
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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