A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655634



Internal ID21603939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78599765..78599765hg38UCSC Ensembl
chr15:78892107..78892107hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082959
SamplesHG00731
Known GenesCHRNA3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655634
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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