A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439783



Internal ID21097336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133554501..133561100hg38UCSC Ensembl
chr10:135368005..135374604hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190433
Samples
Known GenesSYCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439783
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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