A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146213



Internal ID18849734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:90840917..90842818hg38UCSC Ensembl
Outerchr9:93603199..93605100hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999415
SamplesKWB1
Known GenesSYK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146213
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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