A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066959



Internal ID19156178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54215071..54265512hg38UCSC Ensembl
Innerchr19:54718940..54769366hg19UCSC Ensembl
Innerchr19:59410752..59461178hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3850442
hg1950427
hg1850427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3656n100
Supporting Variantsnssv3573328, nssv3726553
Samples
Known GenesLILRA6, LILRB3, LILRB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066959
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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