A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360856



Internal ID22586525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7660375..7660375hg38UCSC Ensembl
chr12:7812971..7812971hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971211
Supporting Variants
Samples
Known GenesAPOBEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360856
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer