A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477779



Internal ID255348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68967203..68968971hg38UCSC Ensembl
chr10:70726959..70728727hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381769
hg191769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035647
Samples
Known GenesDDX21
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477779
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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