A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178926



Internal ID20745966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16333359..16338215hg38UCSC Ensembl
chr17:16236673..16241529hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg384857
hg194857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178926
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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