A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994062



Internal ID20561102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83417101..83426200hg38UCSC Ensembl
chr11:83128144..83137243hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473088
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00943


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