A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134928



Internal ID18908278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:103013188..103013399hg38UCSC Ensembl
Outerchr9:105775470..105775681hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3988436
SamplesKWS1
Known GenesCYLC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134928
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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