A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661049



Internal ID21609354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62893488..62893488hg38UCSC Ensembl
chr15:63185687..63185687hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094917
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661049
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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