A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445554



Internal ID21103107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:108018908..108093629hg38UCSC Ensembl
chr10:109778666..109853387hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3874722
hg1974722
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193135
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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