A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085145



Internal ID21994378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50365500..50365500hg38UCSC Ensembl
chr12:50759283..50759283hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602818
Samples
Known GenesFAM186A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085145
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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