A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953676



Internal ID22728954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110216685..110216685hg38UCSC Ensembl
chr10:111976443..111976443hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357481
Samples
Known GenesMXI1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953676
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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