A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369347



Internal ID22595016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63106903..63127938hg38UCSC Ensembl
chr11:62874375..62895410hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3821036
hg1921036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925763
Supporting Variants
Samples
Known GenesSLC22A24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369347
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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