A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979640



Internal ID22754575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36322283..36322283hg38UCSC Ensembl
chr21:37694581..37694581hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389845
Samples
Known GenesMORC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979640
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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