A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975897



Internal ID22750832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110450831..110450831hg38UCSC Ensembl
chr12:110888636..110888636hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975897
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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