A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936762



Internal ID25224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95679391..95686023hg38UCSC Ensembl
chr3:95398235..95404867hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg386633
hg196633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445132
Supporting Variants
Samples
Known GenesMTHFD2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936762
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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