A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961091



Internal ID18857789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:47746532..47746587hg38UCSC Ensembl
Outerchr11:47768084..47768139hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110683
Supporting Variants
SamplesKWS1
Known GenesFNBP4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961091
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