A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985576



Internal ID20552616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101462975..101466973hg38UCSC Ensembl
chr11:101333706..101337704hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383999
hg193999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473390
Supporting Variants
Samples
Known GenesTRPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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