A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944872



Internal ID30581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187943361..187943458hg38UCSC Ensembl
chr3:187661149..187661246hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436699
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944872
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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