A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451408



Internal ID21108961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98129001..98167700hg38UCSC Ensembl
chr10:99888758..99927457hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3838700
hg1938700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185666
Samples
Known GenesR3HCC1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451408
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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