A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107056



Internal ID21474767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6429025..6429025hg38UCSC Ensembl
chr19:6429036..6429036hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650038
Supporting Variants
SamplesHG03371
Known GenesSLC25A41
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107056
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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