A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182862



Internal ID20749902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4267032..4306754hg38UCSC Ensembl
chr17:4170327..4210049hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3839723
hg1939723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507429
Supporting Variants
Samples
Known GenesUBE2G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182862
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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