A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087324



Internal ID21280808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55202229..55209364hg38UCSC Ensembl
Innerchr8:56114789..56121924hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg387136
hg197136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112352
Supporting Variants
Samplessample302
Known GenesXKR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087324
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