A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060997



Internal ID18803528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54228100..54338192hg38UCSC Ensembl
Innerchr19:54731974..54849463hg19UCSC Ensembl
Innerchr19:59423786..59541275hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38110093
hg19117490
hg18117490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3660n100
Supporting Variantsnssv3573410
Samples
Known GenesLILRA3, LILRA4, LILRA5, LILRA6, 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)nsv1060997
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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