A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604126



Internal ID21552793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41172813..41173570hg38UCSC Ensembl
chr15:41465011..41465768hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085535
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604126
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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