A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066425



Internal ID18808956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54182441..54237431hg38UCSC Ensembl
Innerchr19:54686322..54741307hg19UCSC Ensembl
Innerchr19:59378134..59433119hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3854991
hg1954986
hg1854986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3573312, nssv3573311
Samples
Known GenesLILRA6, LILRB3, MBOAT7, RPS9, TSEN34
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066425
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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