A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435837



Internal ID21093390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94135580..94141841hg38UCSC Ensembl
chr10:95895337..95901598hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg386262
hg196262
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177655
Samples
Known GenesPLCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435837
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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