A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081418



Internal ID21436712
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 StatusS
Merged Variantsnsv5662405
Supporting Variants
SamplesHG00731
Known GenesFAM214A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081418
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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