A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16943264



Internal ID29491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181316762..181316813hg38UCSC Ensembl
chr3:181034550..181034601hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5399397
Supporting Variants
Samples
Known GenesSOX2-OT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16943264
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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