A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647378



Internal ID21595683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84822641..84822641hg38UCSC Ensembl
chr15:85365872..85365872hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092086
SamplesNA12329
Known GenesALPK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647378
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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