A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181835



Internal ID20748875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55675325..55689581hg38UCSC Ensembl
chr17:53752686..53766942hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3814257
hg1914257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181835
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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