A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101885



Internal ID20668925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27101101..27101845hg38UCSC Ensembl
chr3:27142592..27143336hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101885
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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