A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514771



Internal ID20888126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39249644..39260922hg38UCSC Ensembl
chr17:37405897..37417175hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3811279
hg1911279
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177675
Samples
Known GenesFBXL20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514771
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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