A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602767



Internal ID21551426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36800871..36800932hg38UCSC Ensembl
chr15:37093072..37093133hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086445
SamplesHG03371
Known GenesC15orf41, CSNK1A1P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602767
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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