A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351676



Internal ID22577345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65219437..65232919hg38UCSC Ensembl
chr11:64986908..65000390hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3813483
hg1913483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915852
Supporting Variants
Samples
Known GenesSLC22A20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351676
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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