A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993763



Internal ID20560803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63165822..63169369hg38UCSC Ensembl
chr11:62933294..62936841hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg383548
hg193548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474548
Supporting Variants
Samples
Known GenesSLC22A25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993763
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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