A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143234



Internal ID19266850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:109523565..109524282hg38UCSC Ensembl
Outerchr9:112285845..112286562hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984185, nssv3964935
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143234
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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