A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591319



Internal ID21539894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98522525..98522662hg38UCSC Ensembl
chr15:99065754..99065891hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099078
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591319
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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