A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986775



Internal ID20553815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111692401..111693400hg38UCSC Ensembl
chr11:111563125..111564124hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474663
Supporting Variants
Samples
Known GenesSIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986775
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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