A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100702



Internal ID20667742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46405240..46412837hg38UCSC Ensembl
chr3:46446731..46454328hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg387598
hg197598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361735
Supporting Variants
Samples
Known GenesCCRL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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