A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102239



Internal ID20669279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50889501..50890900hg38UCSC Ensembl
chr3:50926932..50928331hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363778
Supporting Variants
Samples
Known GenesDOCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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