A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449195



Internal ID21106748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84230819..84241533hg38UCSC Ensembl
chr10:85990575..86001289hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3810715
hg1910715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192510
Samples
Known GenesLRIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449195
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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