A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443346



Internal ID21100899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120045148..120070515hg38UCSC Ensembl
chr10:121804660..121830027hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3825368
hg1925368
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443346
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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