A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527506



Internal ID22396892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94974965..94975018hg38UCSC Ensembl
chr15:95518194..95518247hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3035n152
Supporting Variantsnssv14375445, nssv14378315
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527506
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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