A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026767



Internal ID21936110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39893977..39894053hg38UCSC Ensembl
chr15:40186178..40186254hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602209
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026767
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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