A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366222



Internal ID22591891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79191967..79192201hg38UCSC Ensembl
chr11:78903012..78903246hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912336
Supporting Variants
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366222
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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