A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455021



Internal ID21112574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129963001..129972000hg38UCSC Ensembl
chr10:131761265..131770264hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv911n223
Supporting Variantsnssv18185400
Samples
Known GenesEBF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455021
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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