A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103869



Internal ID20670909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78599342..78599778hg38UCSC Ensembl
chr3:78648492..78648928hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356757
Supporting Variants
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103869
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00108


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