A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580178



Internal ID16367587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54225610..54242679hg38UCSC Ensembl
Innerchr19:54729478..54746528hg19UCSC Ensembl
Innerchr19:59421290..59438340hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3817070
hg1917051
hg1817051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6555n54
Supporting Variantsnssv901452
Samples
Known GenesLILRA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580178
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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