A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098216



Internal ID20665256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172764838..172765306hg38UCSC Ensembl
chr3:172482628..172483096hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367277
Supporting Variants
Samples
Known GenesECT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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