A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036103



Internal ID21945446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26658819..26661520hg38UCSC Ensembl
chr15:26903966..26906667hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg382702
hg192702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615128
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036103
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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