A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591814



Internal ID21540392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79438268..79438340hg38UCSC Ensembl
chr15:79730610..79730682hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079672
SamplesHG02818
Known GenesKIAA1024
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591814
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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