A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451724



Internal ID21109277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106047159..106548709hg38UCSC Ensembl
chr10:107806917..108308467hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38501551
hg19501551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184753
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451724
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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