A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099657



Internal ID22008890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105437111..105437111hg38UCSC Ensembl
chr12:105830889..105830889hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099657
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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