A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085624



Internal ID21994857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7660375..7660375hg38UCSC Ensembl
chr12:7812971..7812971hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603882
Samples
Known GenesAPOBEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085624
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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