A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645378



Internal ID21593683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78659312..78659312hg38UCSC Ensembl
chr13:79233447..79233447hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084749, nssv17095187
SamplesHG00731, HG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645378
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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