A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926972



Internal ID22702200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44896014..44896814hg38UCSC Ensembl
chr11:44917565..44918365hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv231n209
Supporting Variantsnssv17352771
Samples
Known GenesTSPAN18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926972
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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