A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901492



Internal ID16195448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54227805..54284902hg38UCSC Ensembl
Innerchr19:54731679..54788756hg19UCSC Ensembl
Innerchr19:59423491..59480568hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3857098
hg1957078
hg1857078
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580193
Supporting Variants
Samples
Known GenesLILRA6, LILRB2, LILRB5, MIR4752
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901492
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