A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979418



Internal ID22754353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27062458..27062458hg38UCSC Ensembl
chr15:27307605..27307605hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372829
Samples
Known GenesGABRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979418
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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