A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194943



Internal ID20761983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9002601..9005900hg38UCSC Ensembl
chr17:8905918..8909217hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501133
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194943
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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