A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957182



Internal ID16959369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:46014647..46015022hg38UCSC Ensembl
Outerchr11:46036198..46036573hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004999
SamplesBILGI_BIOE
Known GenesPHF21A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957182
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