A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016414



Internal ID20583454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99395091..99415142hg38UCSC Ensembl
chr13:100047345..100067396hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3820052
hg1920052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485098
Supporting Variants
Samples
Known GenesMIR548AN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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