A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103856



Internal ID20670896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78489738..78494454hg38UCSC Ensembl
chr3:78538888..78543604hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg384717
hg194717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357189
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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