A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420876



Internal ID22478746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47854385..47854505hg38UCSC Ensembl
chr3:47895875..47895995hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902446
Supporting Variants
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420876
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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