A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452789



Internal ID21110342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66147134..66603906hg38UCSC Ensembl
chr10:67906892..68363664hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38456773
hg19456773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv772n223
Supporting Variantsnssv17982442
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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