A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951022



Internal ID16953209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67493430..67504729hg38UCSC Ensembl
Outerchr11:67260901..67272200hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3811300
hg1911300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999570
SamplesBILGI_BIOE
Known GenesPITPNM1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951022
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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