A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657086



Internal ID21605391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40808120..40808120hg38UCSC Ensembl
chr15:41100318..41100318hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097482
SamplesHG00731
Known GenesZFYVE19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657086
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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