A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588249



Internal ID21536810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74798954..74799031hg38UCSC Ensembl
chr15:75091295..75091372hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099144
SamplesNA19239
Known GenesCSK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588249
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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