A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093162



Internal ID20660202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113822201..113833400hg38UCSC Ensembl
chr3:113541048..113552247hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3811200
hg1911200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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