A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056066



Internal ID18798597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54236847..54326343hg38UCSC Ensembl
Innerchr19:54740723..54837615hg19UCSC Ensembl
Innerchr19:59432535..59529427hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3889497
hg1996893
hg1896893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3660n100
Supporting Variantsnssv3573412
Samples
Known GenesLILRA3, 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)nsv1056066
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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