A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649480



Internal ID21597785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95861809..95861809hg38UCSC Ensembl
chr13:96514063..96514063hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092019
SamplesHG03486
Known GenesUGGT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649480
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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