A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987121



Internal ID20554163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116836165..116843710hg38UCSC Ensembl
chr11:116706881..116714426hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg387546
hg197546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472736
Supporting Variants
Samples
Known GenesAPOA1, SIK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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