A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100723



Internal ID20667763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46833942..46863366hg38UCSC Ensembl
chr3:46875432..46904856hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3829425
hg1929425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367905
Supporting Variants
Samples
Known GenesMYL3, PRSS42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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