A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602707



Internal ID21551366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45227375..45229132hg38UCSC Ensembl
chr15:45519573..45521330hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381758
hg191758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082200
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602707
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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