A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994040



Internal ID20561080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83089047..83120857hg38UCSC Ensembl
chr11:82800089..82831899hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3831811
hg1931811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471288
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994040
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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