A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113443



Internal ID18914362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:118929826..118929885hg38UCSC Ensembl
Outerchr11:118800535..118800594hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985623, nssv3970883
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113443
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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