A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148833



Internal ID18849948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:73835108..73837165hg38UCSC Ensembl
Outerchr4:74700825..74702882hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg382058
hg192058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997621
SamplesKWB1
Known GenesCXCL6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148833
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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