A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450546



Internal ID21108099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5444501..5448300hg38UCSC Ensembl
chr10:5486464..5490263hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178535
Samples
Known GenesNET1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450546
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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