A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979608



Internal ID19240372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:98153498..98153574hg38UCSC Ensembl
Outerchr13:98805752..98805828hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142837
Supporting Variants
SamplesKWS2
Known GenesFARP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979608
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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