A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006366



Internal ID20573407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102289572..102290098hg38UCSC Ensembl
chr13:102941922..102942448hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493522
Supporting Variants
Samples
Known GenesFGF14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006366
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0005


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer