A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058409



Internal ID18800940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54336316hg38UCSC Ensembl
Innerchr19:54730202..54847587hg19UCSC Ensembl
Innerchr19:59422014..59539399hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38109988
hg19117386
hg18117386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3660n100
Supporting Variantsnssv3573407, nssv3573408, nssv3726562, nssv3573409
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)nsv1058409
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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