A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154065



Internal ID19195713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:84297946..84304547hg38UCSC Ensembl
Outerchr4:85219099..85225700hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg386602
hg196602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003348
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1154065
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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