A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193217



Internal ID20760257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8859601..8872800hg38UCSC Ensembl
chr10:8901564..8914763hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3813200
hg1913200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193217
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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