A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042360



Internal ID19131579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96471617..96546628hg38UCSC Ensembl
Innerchr11:96204781..96279793hg19UCSC Ensembl
Innerchr11:95844429..95919441hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3875012
hg1975013
hg1875013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1255n100
Supporting Variantsnssv3507185, nssv3504582, nssv3710711, nssv3710712
Samples
Known GenesJRKL-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042360
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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