A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767254



Internal ID20543114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39894056..39894056hg38UCSC Ensembl
chr15:40186257..40186257hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274865
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767254
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer