A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890888



Internal ID168102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156334647..156334682hg38UCSC Ensembl
chr1:156304438..156304473hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5401455
Supporting Variants
Samples
Known GenesCCT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890888
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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