A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153752



Internal ID19199152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:53282937..53301011hg38UCSC Ensembl
Outerchr19:53786190..53804264hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3818075
hg1918075
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002409
SamplesKWB1
Known GenesBIRC8, FAM90A27P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153752
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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