A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940008



Internal ID27393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138264758..138264824hg38UCSC Ensembl
chr3:137983600..137983666hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436421
Supporting Variants
Samples
Known GenesARMC8, NME9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940008
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008898


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