A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067560



Internal ID19156779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54639933..54664828hg38UCSC Ensembl
Innerchr19:55151384..55176279hg19UCSC Ensembl
Innerchr19:59843196..59868091hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3824896
hg1924896
hg1824896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3665n100
Supporting Variantsnssv3573429, nssv3573427, nssv3573430, nssv3573428
Samples
Known GenesLILRB4, MIR8061
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067560
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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