A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101922



Internal ID21267316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15425603..15427468hg38UCSC Ensembl
Innerchr19:15536414..15538279hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381866
hg191866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110371
Supporting Variants
Samplessample110
Known GenesWIZ
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101922
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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