A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149327



Internal ID19202389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92901217..92905518hg38UCSC Ensembl
Outerchr9:95663499..95667800hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384302
hg194302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002837
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149327
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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