A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987195



Internal ID20554237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118536436..118539401hg38UCSC Ensembl
chr11:118407151..118410116hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382966
hg192966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466523
Supporting Variants
Samples
Known GenesTMEM25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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