A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767414



Internal ID18959600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47355548..47358949hg38UCSC Ensembl
chr11:47377099..47380500hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383402
hg193402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075832
Supporting Variants
SamplesKWP1
Known GenesSPI1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767414
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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