A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466226



Internal ID22524116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101505959..101507503hg38UCSC Ensembl
chr11:101376690..101378234hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381545
hg191545
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851968
Supporting Variants
Samples
Known GenesTRPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466226
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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