A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090253



Internal ID21501862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52055634..52055634hg38UCSC Ensembl
chr13:52629770..52629770hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg383183
hg193183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651323
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090253
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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