A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441923



Internal ID21099476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3827988..3831194hg38UCSC Ensembl
chr10:3870180..3873386hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383207
hg193207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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