A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154133



Internal ID18854210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:1992056..1992143hg38UCSC Ensembl
Outerchr19:1992055..1992142hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003409
SamplesKWB1
Known GenesBTBD2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1154133
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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