A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151453



Internal ID19201089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39857581..39860582hg38UCSC Ensembl
Outerchr9:42002599..42005600hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004017
SamplesKWB1
Known GenesKGFLP2, LOC643648
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151453
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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