A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194692



Internal ID20761732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54731874..54753248hg38UCSC Ensembl
chr17:52809235..52830609hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3821375
hg1921375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528745
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194692
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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