A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161236



Internal ID8252834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54654698..54677097hg38UCSC Ensembl
Innerchr19:55166148..55188584hg19UCSC Ensembl
Innerchr19:59857960..59880396hg18UCSC Ensembl
Innerchr19:59857960..59880396hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3822400
hg1922437
hg1822437
hg1722437
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422341
Supporting Variants
SamplesND03746
Known GenesLILRB4
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161236
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer