A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441168



Internal ID21098721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66969745..66981080hg38UCSC Ensembl
chr10:68729503..68740838hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3811336
hg1911336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983938
Samples
Known GenesCTNNA3, LRRTM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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