A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119316



Internal ID19265139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:108499920..108505620hg38UCSC Ensembl
Outerchr9:111262200..111267900hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg385701
hg195701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959754
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119316
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