A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097525



Internal ID21283667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:84688726..84692070hg38UCSC Ensembl
Innerchr1:85154409..85157753hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg383345
hg193345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111364
Supporting Variants
Samplessample348
Known GenesSSX2IP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097525
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