A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509265



Internal ID20882574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58851990..58872414hg38UCSC Ensembl
chr15:59144189..59164613hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg3820425
hg1920425
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186954
Samples
Known GenesFAM63B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509265
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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