A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133383



Internal ID18919264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:118071012..118071072hg38UCSC Ensembl
Outerchr6:118392175..118392235hg19UCSC Ensembl
Cytoband6q22.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3988355
SamplesKWS1
Known GenesSLC35F1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133383
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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