A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919424



Internal ID22694646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34199214..34204493hg38UCSC Ensembl
chr11:34220761..34226040hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385280
hg195280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361966
Samples
Known GenesABTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919424
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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