A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972103



Internal ID22747038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108982839..108982839hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3860
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972103
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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