A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390897



Internal ID21048450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15085905..15875081hg38UCSC Ensembl
chr5:15086014..15875190hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38789177
hg19789177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213294
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390897
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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