A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763778



Internal ID19315145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18462959..18541660hg38UCSC Ensembl
chr13:19037099..19115800hg19UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3878702
hg1978702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076396
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763778
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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