A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859603



Internal ID22634538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101506209..101513003hg38UCSC Ensembl
chr11:101376940..101383734hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg386795
hg196795
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458392
Samples
Known GenesTRPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859603
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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