A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663596



Internal ID21611901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83176939..83176939hg38UCSC Ensembl
chr15:83845691..83845691hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087402
SamplesHG00732
Known GenesHDGFRP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663596
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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