A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085421



Internal ID21456116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25278710..25278710hg38UCSC Ensembl
chr13:25852848..25852848hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653670
Supporting Variants
SamplesHG02492
Known GenesMTMR6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085421
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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