A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106086



Internal ID20673126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86209098..86209571hg38UCSC Ensembl
chr3:86258248..86258721hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371910
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106086
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00465


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