A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098786



Internal ID22008019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42345084..42345084hg38UCSC Ensembl
chr12:42738886..42738886hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg382349
hg192349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601800
Samples
Known GenesPPHLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098786
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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