A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149803



Internal ID19202062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:86087487..86088596hg38UCSC Ensembl
Outerchr8:87099716..87100825hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381110
hg191110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998590
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149803
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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