A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942526



Internal ID22717965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81274595..81277880hg38UCSC Ensembl
chr15:81566936..81570221hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383286
hg193286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382396
Samples
Known GenesIL16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942526
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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