A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994918



Internal ID20561958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84665676..84934197hg38UCSC Ensembl
chr11:84376719..84645241hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38268522
hg19268523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470271
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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