A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984185



Internal ID19241727
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 StatusS
Merged Variantsnsv1143234
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984185
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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