A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997063



Internal ID19189644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:33211158..33211231hg38UCSC Ensembl
Outerchr8:33068676..33068749hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152457
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997063
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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