A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661944



Internal ID21610249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62071970..62071970hg38UCSC Ensembl
chr12:62465751..62465751hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083930
SamplesNA19650
Known GenesFAM19A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661944
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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