A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119864



Internal ID18934044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:18268816..18268870hg38UCSC Ensembl
Outerchr11:18290363..18290417hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982831
SamplesKWS1
Known GenesSAA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119864
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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