A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454439



Internal ID21111992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75024032..75329491hg38UCSC Ensembl
chr10:76783790..77089249hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38305460
hg19305460
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186476
Samples
Known GenesCOMTD1, DUPD1, DUSP13, KAT6B, SAMD8, VDAC2, ZNF503-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454439
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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