A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446223



Internal ID21103776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83953078..83953655hg38UCSC Ensembl
chr10:85712834..85713411hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984577
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446223
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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