A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915913



Internal ID22691131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101466916..101467635hg38UCSC Ensembl
chr11:101337647..101338366hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356595
Samples
Known GenesTRPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915913
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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