A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177675



Internal ID20744715
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 StatusS
Merged Variantsnsv6514771
Supporting Variants
Samples
Known GenesFBXL20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177675
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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