A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387371



Internal ID22445241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20407359..20441575hg38UCSC Ensembl
chr13:20981498..21015714hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3834217
hg1934217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940022
Supporting Variants
Samples
Known GenesCRYL1, MIR4499
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387371
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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