A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587444



Internal ID21536004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26417038..26417089hg38UCSC Ensembl
chr15:26662185..26662236hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095473
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587444
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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