A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574525



Internal ID16015248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:17507716..17519294hg38UCSC Ensembl
Innerchr17:17411030..17422608hg19UCSC Ensembl
Innerchr17:17351755..17363333hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3811579
hg1911579
hg1811579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv868859
Samples
Known GenesPEMT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574525
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer