A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083930



Internal ID21505491
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 StatusS
Merged Variantsnsv5661944
Supporting Variants
SamplesNA19650
Known GenesFAM19A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083930
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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