A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215912



Internal ID20782952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15736333..15948336hg38UCSC Ensembl
chr5:15736442..15948445hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38212004
hg19212004
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385127
Supporting Variants
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215912
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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