A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650268



Internal ID21598573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60350119..60350119hg38UCSC Ensembl
chr15:60642318..60642318hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090927
SamplesNA24385
Known GenesANXA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650268
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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