A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452361



Internal ID21109914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114822501..114827900hg38UCSC Ensembl
chr10:116582260..116587659hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192946
Samples
Known GenesFAM160B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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