A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964005



Internal ID19213081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:139951769..139955612hg38UCSC Ensembl
Outerchr3:139670611..139674454hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg383844
hg193844
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129700
Supporting Variants
SamplesKWS1
Known GenesCLSTN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964005
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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