A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445658



Internal ID21103211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67540001..67540900hg38UCSC Ensembl
chr10:69299759..69300658hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983384
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445658
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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