A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995532



Internal ID20562572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94872546..94874044hg38UCSC Ensembl
chr11:94605711..94607209hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470511
Supporting Variants
Samples
Known GenesAMOTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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