A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952766



Internal ID17301640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:133955806..133956805hg38UCSC Ensembl
Outerchr11:133825701..133826700hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999648
SamplesBILGI_BIOE
Known GenesIGSF9B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952766
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