A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3664n100



Internal ID22789751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54556007..54606995hg38UCSC Ensembl
chr19:55067465..55118460hg19UCSC Ensembl
chr19:59759277..59810272hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3850989
hg1950996
hg1850996
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056888, nsv1059338
Samples
Known GenesLILRA1, LILRA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3664n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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