A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436306



Internal ID21093859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5410601..5415700hg38UCSC Ensembl
chr10:5452564..5457663hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181256
Samples
Known GenesNET1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436306
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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