A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447635



Internal ID21105188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52810827..53021789hg38UCSC Ensembl
chr10:54570587..54781549hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38210963
hg19210963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447635
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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