A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422234



Internal ID7906331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54575991..54728387hg38UCSC Ensembl
Innerchr19:55087458..55239853hg19UCSC Ensembl
Innerchr19:59779270..59931665hg18UCSC Ensembl
Innerchr19:59779270..59931665hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38152397
hg19152396
hg18152396
hg17152396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv17e196
Supporting Variantsessv5161528
SamplesND01666
Known GenesKIR3DL3, LILRA1, LILRA2, LILRB1, LILRB4, LILRP2, MIR8061
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422234
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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