A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645065



Internal ID21593370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74871314..74871314hg38UCSC Ensembl
chr15:75163655..75163655hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087854
SamplesHG03683
Known GenesSCAMP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645065
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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