A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006371



Internal ID20573412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102369205..102369617hg38UCSC Ensembl
chr13:103021555..103021967hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489564
Supporting Variants
Samples
Known GenesFGF14, FGF14-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006371
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00178


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