A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513144



Internal ID20886485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39333227..39337067hg38UCSC Ensembl
chr17:37489480..37493320hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383841
hg193841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191316
Samples
Known GenesFBXL20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513144
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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