A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146436



Internal ID18848361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:101258021..101259056hg38UCSC Ensembl
Outerchr4:102179178..102180213hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381036
hg191036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999640
SamplesKWB1
Known GenesPPP3CA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146436
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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