A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936758



Internal ID25221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95665451..95665502hg38UCSC Ensembl
chr3:95384295..95384346hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5406831
Supporting Variants
Samples
Known GenesMTHFD2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936758
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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