A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663074



Internal ID21611379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113332314..113332314hg38UCSC Ensembl
chr13:113986629..113986629hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095157
SamplesHG02011
Known GenesGRTP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663074
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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