A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100965



Internal ID20668005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5238566..5240593hg38UCSC Ensembl
chr3:5280251..5282278hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg382028
hg192028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361174
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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