A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593811



Internal ID21542402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91811760..91812740hg38UCSC Ensembl
chr15:92354990..92355970hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38981
hg19981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092256
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593811
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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