A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119311



Internal ID19249474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:65767945..65779245hg38UCSC Ensembl
Outerchr9:70386800..70398100hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3811301
hg1911301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959748
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119311
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