A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056967



Internal ID18799498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54212959..54293995hg38UCSC Ensembl
Innerchr19:54716828..54797848hg19UCSC Ensembl
Innerchr19:59408640..59489660hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3881037
hg1981021
hg1881021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3654n100
Supporting Variantsnssv3573313
Samples
Known GenesLILRA6, LILRB2, LILRB3, 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)nsv1056967
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer