A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151558



Internal ID19203261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39865281..39874682hg38UCSC Ensembl
Outerchr9:42010299..42019700hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg389402
hg199402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002985
SamplesKWB1
Known GenesKGFLP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151558
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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