A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952747



Internal ID16954934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:119308591..119317490hg38UCSC Ensembl
Outerchr11:119179301..119188200hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999631
SamplesBILGI_BIOE
Known GenesMCAM, MIR6756
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952747
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