A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003191



Internal ID19192887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:138162147..138202750hg38UCSC Ensembl
Outerchr9:141056599..141093200hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3840604
hg1936602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1153919
Supporting Variants
SamplesKWB1
Known GenesTUBBP5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003191
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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