A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859123



Internal ID22634058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78133637..78135936hg38UCSC Ensembl
chr11:77844683..77846982hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460457
Samples
Known GenesALG8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859123
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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