A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646554



Internal ID21594859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55958936..55958936hg38UCSC Ensembl
chr15:56251134..56251134hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386095
hg196095
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080232
SamplesHG00513
Known GenesNEDD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646554
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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