A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656985



Internal ID21605290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49652608..49652608hg38UCSC Ensembl
chr15:49944805..49944805hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096213
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656985
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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