A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102408



Internal ID20669448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75964101..75965200hg38UCSC Ensembl
chr3:76013252..76014351hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357554
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102408
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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