A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125537



Internal ID18930423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125025001..125025073hg38UCSC Ensembl
Outerchr11:124894897..124894969hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983716
SamplesKWS2
Known GenesCCDC15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125537
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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