A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089057



Internal ID21291508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57811316..58011612hg38UCSC Ensembl
Innerchr10:59571076..59771372hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38200297
hg19200297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115729
Supporting Variants
Samplessample76
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089057
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