A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365437



Internal ID21022990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15640583..15745432hg38UCSC Ensembl
chr4:15642206..15747055hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38104850
hg19104850
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212731
Samples
Known GenesBST1, FAM200B, FBXL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365437
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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