A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098672



Internal ID22007905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29253280..29253280hg38UCSC Ensembl
chr12:29406213..29406213hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608785
Samples
Known GenesFAR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098672
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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