A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148669



Internal ID19201116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40321081..40343782hg38UCSC Ensembl
Outerchr9:42466099..42488800hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3822702
hg1922702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997459
SamplesKWB1
Known GenesFAM95B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148669
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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