A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088129



Internal ID21997362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51825864..51825864hg38UCSC Ensembl
chr12:52219648..52219648hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600585
Samples
Known GenesFIGNL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088129
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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