A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098211



Internal ID20665251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172702713..172704734hg38UCSC Ensembl
chr3:172420503..172422524hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg382022
hg192022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365053
Supporting Variants
Samples
Known GenesNCEH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098211
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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