A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442312



Internal ID21099865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:54138533..54164553hg38UCSC Ensembl
chr10:55898293..55924313hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3826021
hg1926021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190449
Samples
Known GenesPCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442312
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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