A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv636n223



Internal ID22803604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18624051..18634961hg38UCSC Ensembl
chr10:18912980..18923890hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3810911
hg1910911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6438774, nsv6450032
Samples
Known GenesNSUN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv636n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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