A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646262



Internal ID21594567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95942477..95942477hg38UCSC Ensembl
chr15:96485706..96485706hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg386056
hg196056
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087181
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646262
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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