A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930119



Internal ID20824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11415882..11415948hg38UCSC Ensembl
chr3:11457356..11457422hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437011
Supporting Variants
Samples
Known GenesATG7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930119
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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