A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585128



Internal ID21533673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85843417..85843488hg38UCSC Ensembl
chr15:86386648..86386719hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093077
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585128
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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