A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999578



Internal ID17292530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:69493733..69502632hg38UCSC Ensembl
Outerchr11:69308501..69317400hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951031
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999578
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