A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435641



Internal ID21093194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16785481..16908110hg38UCSC Ensembl
chr10:16827480..16950109hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38122630
hg19122630
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194520
Samples
Known GenesCUBN, RSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435641
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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