A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445716



Internal ID21103269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71197245..71475771hg38UCSC Ensembl
chr10:72957002..73235528hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38278527
hg19278527
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191267
Samples
Known GenesCDH23, SLC29A3, UNC5B, UNC5B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445716
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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