A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986758



Internal ID20553798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111408553..111410199hg38UCSC Ensembl
chr11:111279278..111280924hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg381647
hg191647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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