A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086325



Internal ID21487982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52172767..52172767hg38UCSC Ensembl
chr13:52746902..52746902hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658474
Supporting Variants
SamplesNA18534
Known GenesMRPS31P5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086325
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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