A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455446



Internal ID21112999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114333768..114340277hg38UCSC Ensembl
chr10:116093527..116100036hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg386510
hg196510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189374
Samples
Known GenesAFAP1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455446
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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