A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435680



Internal ID21093233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34911162..35291142hg38UCSC Ensembl
chr10:35200090..35580070hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38379981
hg19379981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv685n223
Supporting Variantsnssv18184328
Samples
Known GenesCCNY, CREM, CUL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435680
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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