A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006314



Internal ID20573355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101722621..101723170hg38UCSC Ensembl
chr13:102374971..102375520hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477963
Supporting Variants
Samples
Known GenesFGF14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0005


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