A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986619



Internal ID20553659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118673027..118678259hg38UCSC Ensembl
chr11:118543736..118548968hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385233
hg195233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473362
Supporting Variants
Samples
Known GenesTREH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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