A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101120



Internal ID20668160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25380782..25382414hg38UCSC Ensembl
chr3:25422273..25423905hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381633
hg191633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372127
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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