A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182665



Internal ID20749705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102444680..102447729hg38UCSC Ensembl
chr10:104204437..104207486hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg383050
hg193050
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182665
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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