A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941831



Internal ID22717262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27490027..27491683hg38UCSC Ensembl
chr15:27735173..27736829hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381657
hg191657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377471
Samples
Known GenesGABRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941831
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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