A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096127



Internal ID21268722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57586864..57612826hg38UCSC Ensembl
Innerchr15:57879062..57905024hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3825963
hg1925963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114710
Supporting Variants
Samplessample129
Known GenesGCOM1, MYZAP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096127
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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