A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910903



Internal ID22686115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35752483..35752601hg38UCSC Ensembl
chr11:35774031..35774149hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357647
Samples
Known GenesTRIM44
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910903
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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