A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093302



Internal ID20660342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108295529..108336410hg38UCSC Ensembl
chr3:108014376..108055257hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3840882
hg1940882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369448
Supporting Variants
Samples
Known GenesHHLA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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