A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422341



Internal ID8253124
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 StatusM
Merged Variants
Supporting Variantsessv5161236
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)esv2422341
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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