A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151480



Internal ID19202344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:41186370..41192671hg38UCSC Ensembl
Outerchr9:69259599..69265900hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg386302
hg196302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002908
SamplesKWB1
Known GenesCBWD5, CBWD6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151480
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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