A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442729



Internal ID21100282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34777955..35022755hg38UCSC Ensembl
chr10:35066883..35311683hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38244801
hg19244801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv683n223
Supporting Variantsnssv18183337
Samples
Known GenesCUL2, PARD3, PARD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442729
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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