A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100438



Internal ID20667478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180184886..180186501hg38UCSC Ensembl
chr3:179902674..179904289hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381616
hg191616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359689
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100438
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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