A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444426



Internal ID21101979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16257998..16349206hg38UCSC Ensembl
chr10:16299997..16391205hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3891209
hg1991209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444426
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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