A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059338



Internal ID19148557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54569678..54606995hg38UCSC Ensembl
Innerchr19:55081145..55118460hg19UCSC Ensembl
Innerchr19:59772957..59810272hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3837318
hg1937316
hg1837316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3664n100
Supporting Variantsnssv3573424
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)nsv1059338
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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