A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437435



Internal ID21094988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87483601..87516100hg38UCSC Ensembl
chr10:89243358..89275857hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3832500
hg1932500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv844n223
Supporting Variantsnssv18196559
Samples
Known GenesMINPP1, MIR4678
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437435
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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