A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4000479



Internal ID18846264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:86145214..86145380hg38UCSC Ensembl
Outerchr4:87066367..87066533hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1148441
Supporting Variants
SamplesKWB1
Known GenesMAPK10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4000479
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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