A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652603



Internal ID21600908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33195804..33195804hg38UCSC Ensembl
chr15:33488005..33488005hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382169
hg192169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089140
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652603
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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