A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451251



Internal ID21108804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89744722..89745118hg38UCSC Ensembl
chr10:91504479..91504875hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193087
Samples
Known GenesKIF20B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451251
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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