A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102762



Internal ID21288619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:152436817..152463920hg38UCSC Ensembl
Innerchr1:152409293..152436396hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3827104
hg1927104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112801
Supporting Variants
Samplessample419
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102762
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