A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454765



Internal ID21112318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65714725..65948013hg38UCSC Ensembl
chr10:67474483..67707771hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38233289
hg19233289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192142
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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