A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147606



Internal ID19197323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:151419622..151420510hg38UCSC Ensembl
Outerchr4:152340774..152341662hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996396
SamplesKWB1
Known GenesFAM160A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147606
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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