A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146210



Internal ID18849513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:6297012..6330133hg38UCSC Ensembl
Outerchr19:6297023..6330144hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3833122
hg1933122
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999416
SamplesKWB1
Known GenesACER1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146210
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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