A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146895



Internal ID18854271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:14621549..14623374hg38UCSC Ensembl
Outerchr19:14732361..14734186hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381826
hg191826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998257
SamplesKWB1
Known GenesEMR3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146895
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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