A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587184



Internal ID21535743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60349853..60349906hg38UCSC Ensembl
chr15:60642052..60642105hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084911
SamplesHG03125
Known GenesANXA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587184
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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