A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964011



Internal ID19209593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:182153133..182153263hg38UCSC Ensembl
Outerchr3:181870921..181871051hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143067
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964011
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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