A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024030



Internal ID21933373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37864309..37864371hg38UCSC Ensembl
chr15:38156510..38156572hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024030
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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