A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646658



Internal ID21594963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38988089..38988089hg38UCSC Ensembl
chr13:39562226..39562226hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085825
SamplesHG00513
Known GenesSTOML3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646658
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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