A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648249



Internal ID21596554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:29949845..29949845hg38UCSC Ensembl
chr15:30242048..30242048hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092516
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648249
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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