A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865348



Internal ID22640283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43920557..43929724hg38UCSC Ensembl
chr11:43942107..43951274hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg389168
hg199168
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465699
Samples
Known GenesALKBH3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865348
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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