A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993443



Internal ID20560484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57729934..57730563hg38UCSC Ensembl
chr11:57497406..57498035hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460909
Supporting Variants
Samples
Known GenesTMX2, TMX2-CTNND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993443
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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