A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150718



Internal ID19198011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128130420..128138921hg38UCSC Ensembl
Outerchr9:130892699..130901200hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg388502
hg198502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996189
SamplesKWB1
Known GenesPTGES2-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150718
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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