A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024687



Internal ID20591727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49535274..49540186hg38UCSC Ensembl
chr15:49827471..49832383hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg384913
hg194913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508617
Supporting Variants
Samples
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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