A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146589



Internal ID19198246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:68291783..68319584hg38UCSC Ensembl
Outerchr9:70906699..70934500hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3827802
hg1927802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995745
SamplesKWB1
Known GenesCBWD3, FOXD4L3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146589
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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