A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953852



Internal ID22729121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108690880..108690880hg38UCSC Ensembl
chr5:108026581..108026581hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953852
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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