A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100291



Internal ID20667331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189085077..189087136hg38UCSC Ensembl
chr3:188802866..188804925hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382060
hg192060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367810
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100291
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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