A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064090



Internal ID18806621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54292288hg38UCSC Ensembl
Innerchr19:54730202..54796141hg19UCSC Ensembl
Innerchr19:59422014..59487953hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3865960
hg1965940
hg1865940
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3654n100
Supporting Variantsnssv3573396
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)nsv1064090
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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