A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146168



Internal ID19202036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:67634007..67641444hg38UCSC Ensembl
Outerchr8:68546242..68553679hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg387438
hg197438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999369
SamplesKWB1
Known GenesCPA6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146168
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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