A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658756



Internal ID21607061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68896972..68896972hg38UCSC Ensembl
chr15:69189311..69189311hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090560
SamplesHG02587
Known GenesMIR548H4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658756
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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