A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153690



Internal ID18853600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:109469796..109472297hg38UCSC Ensembl
Outerchr6:109790999..109793500hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002341
SamplesKWB1
Known GenesZBTB24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153690
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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