A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593753



Internal ID21542344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41624414..41624491hg38UCSC Ensembl
chr15:41916612..41916689hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096627
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593753
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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