A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938329



Internal ID26278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112806949..112911606hg38UCSC Ensembl
chr3:112525796..112630453hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38104658
hg19104658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443302
Supporting Variants
Samples
Known GenesCD200R1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938329
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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