A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051819



Internal ID20618860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11663001..11665300hg38UCSC Ensembl
chr1:11723058..11725357hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326379
Supporting Variants
Samples
Known GenesFBXO44, FBXO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051819
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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