A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999081



Internal ID19189250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:28888403..28888465hg38UCSC Ensembl
Outerchr19:29379310..29379372hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151897
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999081
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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