A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350705



Internal ID22576374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84765898..84767709hg38UCSC Ensembl
chr11:84476941..84478752hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921157
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350705
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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