A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098829



Internal ID21267747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:2688760..2712614hg38UCSC Ensembl
Innerchr17:2592054..2615908hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3823855
hg1923855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113860
Supporting Variants
Samplessample116
Known GenesCLUH, MIR6776
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098829
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