A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662405



Internal ID21610710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52674205..52674205hg38UCSC Ensembl
chr15:52966402..52966402hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081418
SamplesHG00731
Known GenesFAM214A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662405
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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