A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006367



Internal ID20573408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102332291..102332853hg38UCSC Ensembl
chr13:102984641..102985203hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479457
Supporting Variants
Samples
Known GenesFGF14, FGF14-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006367
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00035


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