A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891220



Internal ID168330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9670465..9676883hg38UCSC Ensembl
chr1:9730523..9736941hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg386419
hg196419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414091
Supporting Variants
Samples
Known GenesPIK3CD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891220
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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