A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085639



Internal ID20652679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25989979..25997510hg38UCSC Ensembl
chr2:26212848..26220379hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg387532
hg197532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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