A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587982



Internal ID21536543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44288429..44288510hg38UCSC Ensembl
chr15:44580627..44580708hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093290
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587982
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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