A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055860



Internal ID19145079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54282167hg38UCSC Ensembl
Innerchr19:54730202..54786022hg19UCSC Ensembl
Innerchr19:59422014..59477834hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3855839
hg1955821
hg1855821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3657n100
Supporting Variantsnssv3573395
Samples
Known GenesLILRA6, LILRB2, LILRB5, MIR4752
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055860
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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