A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008352



Internal ID20575392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28309169..28311120hg38UCSC Ensembl
chr13:28883306..28885257hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg381952
hg191952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493038
Supporting Variants
Samples
Known GenesFLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008352
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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