A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941594



Internal ID22717021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26658816..26661519hg38UCSC Ensembl
chr15:26903963..26906666hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg382704
hg192704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374260
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941594
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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