A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848140



Internal ID22623075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94123180..94133101hg38UCSC Ensembl
chr11:93856346..93866267hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg389922
hg199922
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468431
Samples
Known GenesPANX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848140
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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